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Thread: Mytrueancestry.com

  1. #2176
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    Salento's Avatar
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    Points: 65,109, Level: 79
    Level completed: 17%, Points required for next Level: 1,341
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    Y-DNA haplogroup
    T1a2 -Z19945
    MtDNA haplogroup
    H12a

    Ethnic group
    Italian
    Country: United States



    3 members found this post helpful.
    You are the #1 top match to this sample! :)

    You are #1 among 895 other users who also have a deep dive match with this sample. This makes your relationship to this individual very unique. Full research for this sample is activated for you regardless of your access level ...


  2. #2177
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    Duarte's Avatar
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    Location
    Belo Horizonte
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    Points: 45,312, Level: 65
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    Y-DNA haplogroup
    R1b-DF27-FGC35133

    Ethnic group
    Portuguese-Brazilian
    Country: Brazil



    MTA - most recent results.


    Code:
    Code:


    I have not any match 100%.

  3. #2178
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    Carlos's Avatar
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    Points: 30,981, Level: 54
    Level completed: 12%, Points required for next Level: 969
    Overall activity: 63.0%

    Y-DNA haplogroup
    E-V22>YF66572
    MtDNA haplogroup
    J1c5c1

    Ethnic group
    España
    Country: Spain



    Kit: Medieval Villa Magna Italy (R63)

    Medical Analysis

    SNP: rs12979860 (CC) - Relevance:9.2
    ~80% of such hepatitis c patients respond to treatment
    SNP: rs9939609 (TA) - Relevance:7.2
    1.3x risk for t2d; obesity risk
    SNP: gs153 (Positive) - Relevance:5.0
    Ultra fast metabolism
    SNP: gs156a (Positive) - Relevance:5.0
    Fast metabolism
    SNP: rs6983267 (GT) - Relevance:3.2
    1.3x risk of prostate cancer; aspirin reduces risk of colorectal cancer
    SNP: rs738409 (CC) - Relevance:2.9
    Higher odds of alcoholic liver disease, increased liver fat
    SNP: rs1042522 (CC) - Relevance:2.8
    Live 3 years longer. chemotherapy is more effective.
    SNP: rs8050136 (CA) - Relevance:2.7
    1.2x increased risk for t2d in some populations
    SNP: rs7412 (CC) - Relevance:2.4
    More likely to gain weight if taking olanzapine
    SNP: rs17782313 (CC) - Relevance:2.2
    Adults likely to be 0.44 bmi units higher
    SNP: rs1061170 (CT) - Relevance:2.1
    2.5x risk for amd; higher mortality among nonagenarians
    SNP: rs13266634 (CC) - Relevance:2.0
    Increased risk for type-2 diabetes
    SNP: rs671 (GG) - Relevance:1.8
    Alcohol flush: normal, doesn\'t flush. normal hangovers. normal risk of alcoholism. normal risk of esophageal cancer. disulfiram is effective for alcoholism.
    SNP: rs2032582 (AA) - Relevance:1.7
    Rare genotype, on a triallelic snp
    SNP: rs53576 (GG) - Relevance:1.6
    Optimistic and empathetic; handle stress well}}the one in four subjects who inherited a variation in this allele called g/g were significantly better at accurately reading the emotions of others by observing their faces than were the remaining three-quarters of subjects, who had inherited either a pair of a's or an a and a g from their parents at this site. compared to the three-fourths with a/a or a/g variations, the g/g individuals were also less likely to startle when blasted by a loud noise, or to become stressed at the prospect of such a noise. and by their own reports, the g/g subjects were mellower and more attuned to other people than were the a/as or a/gs. [http://latimesblogs.latimes.com/boos...-empathy-.html news]-------effect on parental sensitivitycontrolling for maternal education, depression and marital discord, oxtr [f(1,152)=4.32, p=0.04, partial n2=0.03]gene was significantly associated with maternal sensitivity. mothers with oxtr aa or ag genotypes were less sensitive than mothers with the gg genotype. the genetic difference accounts for 3% influence on variation in sensitive parenting. [bakermans-kranenburg mj, van ijzendoorn mh. oxytocin receptor (oxtr) and serotonin transporter (5-htt) genes associated with observed parenting. soc cogn affect neurosci. 2008 jun;3(2):128-34.]in another study, heart rate responses of 40 healthy females without children were measured during the presentation of three episodes of infant cry sounds. participants with the presumably more efficient variant of the oxytonergic system gene (oxtr gg) had more pronounced physiological reactivity to repeated cry sounds, except when they showed more symptoms of depression.[riem mm, pieper s, out d, bakermans-kranenburg mj, van ijzendoorn mh. oxytocin receptor gene and depressive symptoms associated with physiological reactivity to infant crying. soc cogn affect neurosci. 2010 apr 16.][http://newsroom.ucla.edu/portal/ucla...er-215259.aspx optimism]yet another study ({{pmid|19934046|oa=1
    SNP: rs1800562 (GG) - Relevance:1.3
    Not a c282y hemochromatosis carrier.
    SNP: rs7566605 (CC) - Relevance:1.3
    Mixed evidence of increased obesity risk, may suppress excercise effects in men
    SNP: rs1799983 (TG) - Relevance:1.3
    Increased risk of preeclampsia
    SNP: rs3184504 (TT) - Relevance:1.3
    Increased risk for celiac disease
    SNP: rs10811661 (TT) - Relevance:1.3
    1.2x increased risk for type-2 diabetes
    SNP: rs16944 (AA) - Relevance:1.2
    Increased risk for osteoarthritis
    SNP: rs4402960 (GT) - Relevance:1.2
    1.2x increased risk for type-2 diabetes, ~1x risk for gestational diabetes
    SNP: rs401681 (CC) - Relevance:1.1
    ~1.2x increased risk for several types of cancer
    SNP: rs4939827 (TT) - Relevance:1.1
    1x risk for colorectal cancer
    SNP: rs6897932 (CC) - Relevance:1.1
    1.5x increased risk for multiple sclerosis
    SNP: rs12913832 (AA) - Relevance:1.0
    Brown eye color, 80% of the time
    SNP: rs599839 (AA) - Relevance:1.0
    1.4x increased risk for heart disease
    SNP: rs6311 (CC) - Relevance:0.9
    3.6x increased risk of sexual dysfunction when taking ssri antidepressants.
    SNP: rs5219 (TT) - Relevance:0.8
    2.5x increased risk for type-2 diabetes
    SNP: rs17070145 (CC) - Relevance:0.8
    Reduced memory abilities
    SNP: rs9340799 (AA) - Relevance:0.8
    Women have lower risk of endometriosis but normal risk for endometrial cancer, and more cognitive impairment with age.
    SNP: rs9923231 (CT) - Relevance:0.8
    Reduced warfarin dose if treated for vte
    SNP: rs2200733 (CC) - Relevance:0.8
    0.86x decreased risk of atrial fibrillation
    SNP: rs1042713 (GA) - Relevance:0.8
    1.3x increased risk that pediatric inhaler use may make asthma worse
    SNP: rs7756992 (AG) - Relevance:0.8
    1.3x increased risk for type-2 diabetes
    SNP: rs1799971 (AG) - Relevance:0.8
    Stronger cravings for alcohol. if alcoholic, naltrexone treatment 2x more successful
    SNP: rs2230199 (GC) - Relevance:0.8
    1.6x+ risk of armd
    SNP: rs16891982 (GG) - Relevance:0.8
    Generally european; light skin; possibly an increased risk of melanoma}}this snp is associated with skin, hair, and eye colour, and risk of melanoma. individuals with the g;g genotype are generally of european descent and have fair skin.{{pmid auto|pmid=19710684|oa=1
    SNP: rs5186 (AC) - Relevance:0.7
    ~1.4x increased risk of hypertension
    SNP: rs4343 (GG) - Relevance:0.7
    Usually the ace alu deletion; better strength vs endurance;
    SNP: rs4570625 (GG) - Relevance:0.7
    Maybe: higher scores on anxiety-related personality traits; greater placebo response}}one study of (only) 25 people {{pmid|19052197
    SNP: rs1048661 (GG) - Relevance:0.7
    Possibly higher glaucoma risk?
    SNP: rs7517847 (GG) - Relevance:0.7
    0.65x reduced risk for crohn's disease
    SNP: rs7923837 (GA) - Relevance:0.7
    1.6x risk for t2d
    SNP: rs10889677 (CC) - Relevance:0.7
    1x increased risk for certain autoimmune diseases; 2.3x increased risk for graves disease
    SNP: rs505922 (TT) - Relevance:0.7
    Blood type o
    SNP: rs6280 (CC) - Relevance:0.7
    Better response to olanzapine
    SNP: rs266729 (CG) - Relevance:0.7
    0.73x decreased risk for colorectal cancer
    SNP: rs1143679 (GA) - Relevance:0.6
    1.78x increased risk for sle
    SNP: rs12970134 (AA) - Relevance:0.6
    Adult waist 1.8cm larger on average
    SNP: rs889312 (CC) - Relevance:0.6
    Very slightly higher risk for breast cancer
    SNP: rs9652490 (AA) - Relevance:0.6
    ~2x increased risk for parkinson's disease, and, essential tremor
    SNP: rs2943641 (CC) - Relevance:0.6
    Increased risk for type 2 diabetes
    SNP: rs1042714 (GC) - Relevance:0.6
    Complex; see details for increased risks
    SNP: rs2275913 (GA) - Relevance:0.6
    1.4x increased gastric cancer risk. increased risk of acute graft-versus-host disease after unrelated bone marrow transplantation
    SNP: rs1426654 (AA) - Relevance:0.6
    Probably light-skinned, european ancestry
    SNP: rs17576 (GG) - Relevance:0.6
    Higher risk for lung cancer, and copd in smokers; normal risk for mi
    SNP: rs763361 (TT) - Relevance:0.6
    Increased risk for multiple autoimmune diseases
    SNP: rs5498 (AG) - Relevance:0.6
    0.6x decreased risk for diabetic nephropathy in females with type-1 diabetes; 1.9x increased malaria risk
    SNP: rs334558 (AA) - Relevance:0.5
    Later onset of bipolar disorder
    SNP: rs174546 (CT) - Relevance:0.5
    Triglycerides
    SNP: rs3025058 (AA) - Relevance:0.5
    5a/5a; higher mi risk?
    SNP: rs7578597 (TT) - Relevance:0.5
    Type 2 diabetes
    SNP: rs13387042 (AA) - Relevance:0.5
    1.24x increased risk for breast cancer
    SNP: rs7138803 (GG) - Relevance:0.5
    Body mass index
    SNP: rs3761847 (GA) - Relevance:0.5
    1.32 x risk of rheumatoid arthritis.
    SNP: rs703842 (AA) - Relevance:0.5
    Multiple sclerosis
    SNP: rs356219 (GG) - Relevance:0.5
    1.6x increased risk for parkinson's disease
    SNP: rs4307059 (CC) - Relevance:0.5
    Reduced autism risk
    SNP: rs1800947 (CC) - Relevance:0.5
    Lower crp levels
    SNP: rs7647305 (CC) - Relevance:0.5
    Obesity risk
    SNP: rs762551 (CA) - Relevance:0.5
    Carrier of one cyp1a2*1f allele; slow caffeine metabolizer.
    SNP: rs12708716 (AG) - Relevance:0.5
    1.2x risk of type-1 diabetes
    SNP: rs8176719 (TT) - Relevance:0.4
    Likely to be of blood type o
    SNP: rs9934438 (AA) - Relevance:0.4
    Coumadin resistance
    SNP: rs5882 (AA) - Relevance:0.4
    Faster aging. increased risk for dementia. less good cholesterol.
    SNP: rs17465637 (CC) - Relevance:0.4
    1.34x higher risk for myocardial infarction
    SNP: rs5370 (TT) - Relevance:0.4
    Possibly lower hdl cholesterol in women
    SNP: rs2237895 (AA) - Relevance:0.4
    Type 2 diabetes
    SNP: rs1535 (AG) - Relevance:0.4
    4+ iq points for breastfeeding
    SNP: rs2815752 (AA) - Relevance:0.4
    Body mass index
    SNP: rs7927894 (CC) - Relevance:0.4
    0.83x lower risk of atopic dermatitis.
    SNP: rs225014 (CC) - Relevance:0.4
    Hypothyroid patients might benefit from combination t4/t3 therapy (?)
    SNP: rs402710 (CC) - Relevance:0.4
    Common, but higher lung cancer risk ?
    SNP: rs6887695 (GG) - Relevance:0.4
    1.4x increased risk of psoriasis, psoriatic arthritis
    SNP: rs1800972 (GG) - Relevance:0.4
    Reduced risk for crohns disease; reduced risk for maternal hiv transmission
    SNP: rs12248560 (TT) - Relevance:0.4
    Cyp2c19*17 ultra fast metabolizer; drug metabolism effects; also 0.77x decreased breast cancer risk
    SNP: rs4444235 (TT) - Relevance:0.4
    Colorectal cancer
    SNP: rs12980275 (AA) - Relevance:0.4
    Lipid levels in hepatitis C treatment
    SNP: rs2071746 (TT) - Relevance:0.4
    May be part of gs124
    SNP: rs1470579 (CC) - Relevance:0.4
    1.2x increased risk for type-2 diabetes
    SNP: rs4961 (GT) - Relevance:0.4
    1.8x increased risk for high blood pressure
    SNP: rs3764650 (TG) - Relevance:0.4
    Late onset?
    SNP: rs5065 (AA) - Relevance:0.4
    1.12x risk on diuretic; if hypertensive, better outcome when treated with calcium channel blocker than with diuretic
    SNP: rs965513 (AA) - Relevance:0.4
    3.5x increased thyroid cancer risk
    SNP: rs12143842 (CT) - Relevance:0.4
    4.4ms qt interval duration increase on average
    SNP: rs10246939 (TC) - Relevance:0.4
    Can taste bitter
    SNP: rs1495741 (GG) - Relevance:0.4
    Nat2 rapid metabolizer (predicted)
    SNP: rs3817198 (TT) - Relevance:0.4
    Breast cancer
    SNP: rs6259 (GG) - Relevance:0.4
    Best inverse correlation between tea-drinking, soy-consuming premenopausal women and risk of endometrial cancer
    SNP: rs4633 (CT) - Relevance:0.4
    Higher risk for endometrial cancer
    SNP: rs13361189 (TC) - Relevance:0.4
    1.3x increased risk for crohn's disease
    SNP: rs613872 (GT) - Relevance:0.4
    ~5 fold higher risk for fuchs\' dystrophy, a corneal disorder
    SNP: rs7341475 (GG) - Relevance:0.4
    1.58x increased schizophrenia risk for women
    SNP: rs10883365 (GA) - Relevance:0.4
    1.2x increased risk for developing crohn's disease
    SNP: rs2494732 (TT) - Relevance:0.4
    Lower odds of psychosis
    SNP: rs4072037 (CC) - Relevance:0.4
    Magnesium levels
    SNP: rs2251746 (CC) - Relevance:0.4
    Lowest ige levels

    I will put it in several parts because it does not load it completely.

  4. #2179
    Regular Member Achievements:
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    Carlos's Avatar
    Join Date
    26-09-11
    Posts
    2,078
    Points
    30,981
    Level
    54
    Points: 30,981, Level: 54
    Level completed: 12%, Points required for next Level: 969
    Overall activity: 63.0%

    Y-DNA haplogroup
    E-V22>YF66572
    MtDNA haplogroup
    J1c5c1

    Ethnic group
    España
    Country: Spain



    Kit: Medieval Villa Magna Italy (R63)

    SNP: rs10505477 (AG) - Relevance:0.4
    Colorectal cancer
    SNP: rs17822931 (CC) - Relevance:0.4
    Wet earwax. normal body odour. normal colostrum.
    SNP: rs9642880 (GG) - Relevance:0.3
    Slightly lower risk of bladder cancer.
    SNP: rs2420946 (TC) - Relevance:0.3
    1.20x risk for breast cancer
    SNP: rs2304256 (CA) - Relevance:0.3
    1.6x increased risk for sle
    SNP: rs2383207 (AG) - Relevance:0.3
    Increased risk for heart disease
    SNP: rs10838738 (GG) - Relevance:0.3
    Body mass index
    SNP: rs7294919 (TT) - Relevance:0.3
    Average hippocampal volume
    SNP: rs7529229 (TT) - Relevance:0.3
    2.5x lower risk for multiple myeloma versus cc
    SNP: rs7539542 (CC) - Relevance:0.3
    0.51x decreased breast cancer risk
    SNP: rs872071 (GG) - Relevance:0.3
    ~1.5x increased risk for chronic lymphocytic leukemia
    SNP: rs4977756 (GA) - Relevance:0.3
    1.2x higher risk for glioma development
    SNP: rs4553808 (AG) - Relevance:0.3
    Possibly lower risk for myasthenia gravis
    SNP: rs31489 (CC) - Relevance:0.3
    Increased risk for lung cancer and emphysema}}{{pmid auto|pmid=21622582|title=the tert-clptm1l locus for lung cancer predisposes to bronchial obstruction and emphysema
    SNP: rs12807809 (TT) - Relevance:0.3
    Schizophrenia
    SNP: rs6060369 (CC) - Relevance:0.3
    0.88cm taller
    SNP: rs3020314 (CT) - Relevance:0.3
    0.64x reduced lymphoma risk
    SNP: rs689 (TT) - Relevance:0.3
    Type 1 diabetes autoantibodies
    SNP: rs9300039 (CC) - Relevance:0.3
    >1.5x risk for t2d
    SNP: rs6564851 (TG) - Relevance:0.3
    Higher beta-carotene levels
    SNP: rs1049296 (CC) - Relevance:0.3
    C1 subtype of transferrin; common in clinvar
    SNP: rs356220 (TT) - Relevance:0.3
    Increased risk of parkinson's disease
    SNP: rs3846662 (AG) - Relevance:0.3
    LDL cholesterol
    SNP: rs1800860 (AA) - Relevance:0.3
    10% smaller kidneys as newborns
    SNP: rs11218350 (TT) - Relevance:0.3
    0.83x risk for alzheimers
    SNP: rs28940580 (CC) - Relevance:0.3
    Can be ignored for now
    SNP: rs9834312 (GG) - Relevance:0.3
    Taller
    SNP: rs4775041 (GG) - Relevance:0.3
    Highest phosphatidylethanolamine values
    SNP: rs11249433 (GG) - Relevance:0.3
    Breast cancer
    SNP: rs6687758 (AA) - Relevance:0.3
    Colorectal cancer
    SNP: rs63751449 (TT) - Relevance:0.3
    Lynch syndrome; hereditary nonpolyposis colorectal cancer-1
    SNP: rs63749811 (TT) - Relevance:0.3
    Lynch syndrome; hereditary nonpolyposis colorectal cancer (hnpcc1)
    SNP: rs3774426 (CC) - Relevance:0.3
    Better response to certain calcium channel blockers
    SNP: rs1837253 (TT) - Relevance:0.3
    Reduced risk (0.73) for late-onset (adult) asthma
    SNP: rs2546890 (AA) - Relevance:0.3
    Higher risk of multiple sclerosis
    SNP: rs7794745 (TT) - Relevance:0.3
    Slightly increased risk for autism
    SNP: rs896854 (TC) - Relevance:0.3
    Type 2 diabetes
    SNP: rs1805388 (AA) - Relevance:0.3
    Reduced risk of multiple myeloma
    SNP: rs7495174 (AA) - Relevance:0.3
    Blue/gray eyes more likely
    SNP: rs13333226 (AA) - Relevance:0.3
    Common but slightly higher risk for hypertension
    SNP: rs8050894 (CG) - Relevance:0.3
    Average warfarin response (~5 mg/day)
    SNP: rs4464148 (CC) - Relevance:0.3
    1.35x increased risk for colorectal cancer
    SNP: rs8170 (GG) - Relevance:0.3
    Breast cancer
    SNP: rs440446 (GG) - Relevance:0.3
    Increased risk in men for biliary conditions
    SNP: rs610604 (TT) - Relevance:0.2
    Psoriasis
    SNP: rs4917014 (GG) - Relevance:0.2
    Systemic lupus erythematosus
    SNP: rs1800858 (GG) - Relevance:0.2
    May predispose somehow to hirschsprung disease
    SNP: rs231362 (AG) - Relevance:0.2
    Type 2 diabetes
    SNP: rs4355801 (GG) - Relevance:0.2
    Bone mineral density
    SNP: rs12608932 (AA) - Relevance:0.2
    Amyotrophic lateral sclerosis
    SNP: rs4925386 (CC) - Relevance:0.2
    Colorectal cancer
    SNP: rs1410996 (GA) - Relevance:0.2
    Age-related macular degeneration
    SNP: rs6435862 (GG) - Relevance:0.2
    2.8x higher risk of aggressive neuroblastoma
    SNP: rs17388568 (GA) - Relevance:0.2
    1.3x risk of type-1 diabetes
    SNP: rs7837688 (GG) - Relevance:0.2
    1.7x increased risk for prostate cancer
    SNP: rs1954787 (CC) - Relevance:0.2
    ~10% more likely to respond to citalopram
    SNP: rs1012053 (CA) - Relevance:0.2
    0.625x reduced risk of bipolar disorde

  5. #2180
    Regular Member Achievements:
    Veteran25000 Experience PointsThree Friends
    Carlos's Avatar
    Join Date
    26-09-11
    Posts
    2,078
    Points
    30,981
    Level
    54
    Points: 30,981, Level: 54
    Level completed: 12%, Points required for next Level: 969
    Overall activity: 63.0%

    Y-DNA haplogroup
    E-V22>YF66572
    MtDNA haplogroup
    J1c5c1

    Ethnic group
    España
    Country: Spain



    Kit: Medieval Villa Magna Italy (R63)

    SNP: rs602662 (GG) - Relevance:0.2
    Lower vitamin b12 levels
    SNP: rs2180439 (CC) - Relevance:0.2
    Reduced risk of male pattern baldness.
    SNP: rs7014346 (AA) - Relevance:0.2
    Colorectal cancer
    SNP: rs7850258 (AA) - Relevance:0.2
    Slightly lower odds of developing primary hypothyroidism.
    SNP: rs3793784 (GC) - Relevance:0.2
    1.5x risk for armd
    SNP: rs12896399 (GG) - Relevance:0.2
    Light hair color
    SNP: rs11634397 (GG) - Relevance:0.2
    Type 2 diabetes
    SNP: rs8042680 (AA) - Relevance:0.2
    Type 2 diabetes
    SNP: rs4785763 (AC) - Relevance:0.2
    1.5x higher risk for melanoma
    SNP: rs1160312 (GG) - Relevance:0.2
    Reduced risk of baldness.
    SNP: rs2250889 (CC) - Relevance:0.2
    1.69x higher risk for lung cancer
    SNP: rs509749 (AA) - Relevance:0.2
    Common; slight increase in sle risk
    SNP: rs1061147 (CC) - Relevance:0.2
    Reduced 0.34x risk of age related macular degeneration.
    SNP: rs6691170 (GG) - Relevance:0.2
    Colorectal cancer
    SNP: rs10210302 (TT) - Relevance:0.2
    1.8x risk
    SNP: rs13316193 (TT) - Relevance:0.2
    Slight evidence indicating decreased oxtr expression, higher risk of depression, higher risk of autism spectrum disorder.}}{{pmid|22357335}} the association between oxytocin receptor gene polymorphism (oxtr) and trait empathy.{{pmid|17893705}} association between the oxytocin receptor (oxtr) gene and autism: relationship to vineland adaptive behavior scales and cognition.{{pmid|20346758}} genetics of human social behavior.{{pmid|22285934}} oxytocin and social affiliation in humans.{{pmid|23325323
    SNP: rs6812193 (CC) - Relevance:0.2
    Slightly higher risk of developing parkinson's disease for caucasians
    SNP: rs10260404 (TC) - Relevance:0.2
    1.20x risk of developing als
    SNP: rs1793004 (GG) - Relevance:0.2
    0.89x decreased risk for crohn's disease
    SNP: rs931127 (AA) - Relevance:0.2
    2.15x more likely positive lymph node
    SNP: rs7101429 (AA) - Relevance:0.2
    Higher alzheimer's risk if apoe4 also present
    SNP: rs974819 (CC) - Relevance:0.2
    Coronary heart disease
    SNP: rs17580 (TT) - Relevance:0.2
    A slightly reduced functionality form of alpha-1 antitrypsin deficiency
    SNP: rs1676486 (AG) - Relevance:0.2
    1.4x risk for ldh
    SNP: rs243021 (GG) - Relevance:0.2
    Type 2 diabetes
    SNP: rs766432 (AA) - Relevance:0.2
    Beta thalassemia/hemoglobin E disease
    SNP: rs2056202 (CC) - Relevance:0.2
    Common but increased risk of autism
    SNP: rs1554483 (GG) - Relevance:0.2
    1.8x higher risk for obesity if in haplotype
    SNP: rs10069690 (CT) - Relevance:0.2
    Breast cancer
    SNP: rs865686 (GG) - Relevance:0.2
    Breast cancer
    SNP: rs1537415 (GG) - Relevance:0.2
    2x increased risk for periodontitis
    SNP: rs11169552 (CC) - Relevance:0.2
    Colorectal cancer
    SNP: rs7172432 (AA) - Relevance:0.2
    Type 2 diabetes
    SNP: rs2165241 (TC) - Relevance:0.2
    4.4x increased risk of exfoliation glaucoma
    SNP: rs4939883 (CC) - Relevance:0.2
    Associated with higher hdl cholesterol
    SNP: rs12044852 (CC) - Relevance:0.2
    >1.24x risk
    SNP: rs1126497 (TT) - Relevance:0.2
    1.4x increased risk for breast cancer
    SNP: rs182549 (CC) - Relevance:0.2
    Possibly lactose intolerant
    SNP: rs6445975 (GG) - Relevance:0.2
    Disease risk associated
    SNP: rs4864548 (GG) - Relevance:0.2
    1.8x higher risk for obesity if in haplotype
    SNP: rs5335 (GG) - Relevance:0.2
    >1.19x risk for hypertension
    SNP: rs4730751 (AA) - Relevance:0.2
    For kidney donors, 2x more likely to result in allograft rejection
    SNP: rs2383208 (AA) - Relevance:0.2
    Type 2 diabetes
    SNP: rs11246226 (CC) - Relevance:0.2
    Decreased risk of schizophrenia in limited study
    SNP: rs10784502 (CC) - Relevance:0.2
    Better intracranial volume. 2 teaspoons increased cranial capacity and higher IQ
    SNP: rs4344 (GG) - Relevance:0.2
    Faster responder
    SNP: rs4654748 (CC) - Relevance:0.2
    2.90 ng/ml lower vitamin b6 blood concentration|allele1=c|allele2=c
    SNP: rs2802292 (TT) - Relevance:0.2
    Less likely to live to 100.
    SNP: rs7853989 (GG) - Relevance:0.2
    Not blood group b
    SNP: rs4253208 (GG) - Relevance:0.2
    Possible cockayne syndrome, type b
    SNP: rs11045585 (AA) - Relevance:0.2
    24% chance (lower than average) of docetaxel-induced leukopenia/neutropenia
    SNP: rs1047781 (AA) - Relevance:0.2
    Abh blood group "secretor" status if japanese
    SNP: rs7538876 (AA) - Relevance:0.2
    1.28x increased basal cell carcinoma risk.
    SNP: rs10735781 (GC) - Relevance:0.2
    1.11x risk
    SNP: rs3738919 (CC) - Relevance:0.2
    1.94x risk of developing rheumatoid arthritis
    SNP: rs2952768 (TC) - Relevance:0.2
    Slightly less drug dependence, decreased effectiveness of analgesics
    SNP: rs3775948 (GG) - Relevance:0.2
    Slightly higher risk for gout
    SNP: rs1800462 (CC) - Relevance:0.2
    Incapable of detoxifying
    SNP: rs793862 (AG) - Relevance:0.2
    Increased dyslexia risk
    SNP: rs17584499 (CC) - Relevance:0.2
    Type 2 diabetes
    SNP: rs7127900 (GG) - Relevance:0.2
    Prostate cancer
    SNP: rs11037909 (TT) - Relevance:0.2
    1.47x type ii diabetes risk
    SNP: rs1495377 (GC) - Relevance:0.2
    1.3x risk type-2 diabetes
    SNP: rs1545843 (AA) - Relevance:0.2
    1.4x increased risk for depression (for those under 55)
    SNP: rs6495446 (CC) - Relevance:0.2
    2.5x increased risk for chronic kidney disease
    SNP: rs3743930 (CC) - Relevance:0.2
    Some reports of familial mediterranean fever
    SNP: rs1864163 (GG) - Relevance:0.2
    Associated with higher hdl cholesterol
    SNP: rs4359 (TT) - Relevance:0.2
    Faster responder
    SNP: rs6700125 (TC) - Relevance:0.2
    1.2x increased risk for als
    SNP: rs1514175 (AG) - Relevance:0.2
    Body mass index
    SNP: rs4112788 (GG) - Relevance:0.2
    Psoriasis
    SNP: rs7349332 (CC) - Relevance:0.2
    Straighter hair; common
    SNP: rs6458307 (CC) - Relevance:0.2
    1.4x risk
    SNP: rs4870044 (TT) - Relevance:0.2
    Bone mineral density (spine)
    SNP: rs748404 (TT) - Relevance:0.2
    Slightly increased risk (1.25) for lung cancer
    SNP: rs2241423 (GG) - Relevance:0.2
    Body mass index
    SNP: rs12444979 (CC) - Relevance:0.2
    Body mass index
    SNP: rs8055236 (GG) - Relevance:0.2
    Common, but 2.2x higher risk for heart disease
    SNP: rs10423928 (TT) - Relevance:0.2
    Two-hour glucose challenge
    SNP: rs5746059 (AA) - Relevance:0.1
    Slightly higher fat mass
    SNP: rs2205960 (GT) - Relevance:0.1
    Systemic lupus erythematosus
    SNP: rs28997576 (CC) - Relevance:0.1
    Probably increased risk of breast cancer

  6. #2181
    Regular Member Achievements:
    Veteran25000 Experience PointsThree Friends
    Carlos's Avatar
    Join Date
    26-09-11
    Posts
    2,078
    Points
    30,981
    Level
    54
    Points: 30,981, Level: 54
    Level completed: 12%, Points required for next Level: 969
    Overall activity: 63.0%

    Y-DNA haplogroup
    E-V22>YF66572
    MtDNA haplogroup
    J1c5c1

    Ethnic group
    España
    Country: Spain



    Kit: Medieval Villa Magna Italy (R63)

    SNP: rs10513789 (TT) - Relevance:0.1
    Very common. normal risk of parkinson's disease.
    SNP: rs27388 (AA) - Relevance:0.1
    Increased risk of developing schizophrenia
    SNP: rs2327832 (AA) - Relevance:0.1
    Celiac disease
    SNP: rs2073963 (GG) - Relevance:0.1
    Increased risk of baldness
    SNP: rs326 (AA) - Relevance:0.1
    Lower hdl cholesterol
    SNP: rs10958409 (GA) - Relevance:0.1
    1.37x increased aneurysm risk
    SNP: rs12340895 (CG) - Relevance:0.1
    Increased odds (2 fold?) of developing v617f-positive mpn
    SNP: rs10984447 (AA) - Relevance:0.1
    >1.17x increased risk for multiple sclerosis
    SNP: rs1800169 (GG) - Relevance:0.1
    Greater relative benefit of iloperidone to schizophrenics
    SNP: rs7931342 (TG) - Relevance:0.1
    Prostate cancer
    SNP: rs4585 (TT) - Relevance:0.1
    Slightly poorer (0.75x) response to metformin in type 2 diabetics
    SNP: rs11842874 (AA) - Relevance:0.1
    Common but +17% risk osteoarthritis }}risk 1.17 [1.111.23], p = 2.1 108 {{pmid|21871595
    SNP: rs7183877 (CC) - Relevance:0.1
    Blue eye color if part of blue eye color haplotype
    SNP: rs17367504 (GG) - Relevance:0.1
    Reduction in blood pressure
    SNP: rs2077119 (TG) - Relevance:0.1
    0.91x decreased risk for t2d
    SNP: rs4833103 (AC) - Relevance:0.1
    0.75x decreased risk for non-hodgkin's lymphoma
    SNP: rs12500426 (AC) - Relevance:0.1
    Prostate cancer
    SNP: rs12653946 (TT) - Relevance:0.1
    Prostate cancer
    SNP: rs10096633 (CC) - Relevance:0.1
    Triglycerides
    SNP: rs7816345 (CC) - Relevance:0.1
    bigger breast size (normal in european)
    SNP: rs7027989 (AA) - Relevance:0.1
    1.26x increased myocardial infarction risk
    SNP: rs1412829 (AA) - Relevance:0.1
    Glioma (high-grade)
    SNP: rs224136 (CC) - Relevance:0.1
    Crohn's disease
    SNP: rs7091565 (TT) - Relevance:0.1
    1.26x risk of sarcoidosis
    SNP: rs4474514 (AA) - Relevance:0.1
    >3x increased testicular cancer risk for men
    SNP: rs1522305 (GG) - Relevance:0.1
    Slightly increased risk for schizophrenia
    SNP: rs4773144 (GG) - Relevance:0.1
    Coronary heart disease
    SNP: rs4794067 (CC) - Relevance:0.1
    2.1x risk for aspirin induced asthma. but possibly lower risk of lupus and intractable graves\' disease.
    SNP: rs6690993 (AA) - Relevance:0.1
    0.7x decreased risk for als
    SNP: rs3753841 (GG) - Relevance:0.1
    Glaucoma (primary open-angle)
    SNP: rs2144300 (TT) - Relevance:0.1
    HDL cholesterol
    SNP: rs17672135 (TT) - Relevance:0.1
    1.3x risk
    SNP: rs10192566 (CG) - Relevance:0.1
    If diabetic, better response to rosiglitazone
    SNP: rs2310173 (TT) - Relevance:0.1
    Ulcerative colitis
    SNP: rs6718526 (CC) - Relevance:0.1
    1.9x risk of type-2 diabetes
    SNP: rs4276227 (CC) - Relevance:0.1
    1.5x risk
    SNP: rs6797312 (AA) - Relevance:0.1
    2x higher stroke risk in caucasian women
    SNP: rs7679673 (CA) - Relevance:0.1
    Prostate cancer
    SNP: rs7659604 (CT) - Relevance:0.1
    1.4x risk
    SNP: rs7439293 (GA) - Relevance:0.1
    Increased risk of coronary heart disease; better response to statins
    SNP: rs10036748 (CC) - Relevance:0.1
    Systemic lupus erythematosus
    SNP: rs2076295 (TT) - Relevance:0.1
    Common/normal (higher levels of dsp expression)
    SNP: rs4712653 (TT) - Relevance:0.1
    2x increased risk for neuroblastoma
    SNP: rs9295536 (CA) - Relevance:0.1
    Possible increased risk for neuroblastoma
    SNP: rs7753394 (CC) - Relevance:0.1
    1.5x risk of crohn's disease
    SNP: rs13208776 (GG) - Relevance:0.1
    Higher risk for generalized vitiligo
    SNP: rs7787082 (GG) - Relevance:0.1
    7x less likely to respond to certain antidepressants
    SNP: rs10248420 (AA) - Relevance:0.1
    7x less likely to respond to certain antidepressants
    SNP: rs705381 (TC) - Relevance:0.1
    Less likely to gain weight if taking risperidone
    SNP: rs4986782 (AA) - Relevance:0.1
    Slow acetylator = higher risk of smoking-induced lung cancer
    SNP: rs13702 (TT) - Relevance:0.1
    HDL Cholesterol - Triglycerides (HDLC-TG)
    SNP: rs495828 (GG) - Relevance:0.1
    Venous thromboembolism
    SNP: rs6601764 (CC) - Relevance:0.1
    1.52x increased risk of developing crohn's disease
    SNP: rs12184413 (TT) - Relevance:0.1
    0.7x decreased risk for breast cancer
    SNP: rs10772420 (GG) - Relevance:0.1
    Less intense perception of quinine
    SNP: rs3782179 (CC) - Relevance:0.1
    9x lower odds of testicular cancer
    SNP: rs10774625 (AA) - Relevance:0.1
    Retinal vascular caliber
    SNP: rs767603 (CC) - Relevance:0.1
    0.63x reduced risk for intracranial aneurysm
    SNP: rs11622475 (CC) - Relevance:0.1
    1.5x risk of bipolar disorder
    SNP: rs4778241 (AC) - Relevance:0.1
    Usually brown eye color
    SNP: rs8042374 (GG) - Relevance:0.1
    Lung cancer
    SNP: rs12597511 (CT) - Relevance:0.1
    Slightly higher blood pressure
    SNP: rs16953002 (GG) - Relevance:0.1
    Slightly lower risk of melanoma in individuals with low bmi
    SNP: rs4792311 (AA) - Relevance:0.1
    Increased risk of prostate cancer
    SNP: rs11650354 (TT) - Relevance:0.1
    8x risk for allergic asthma
    SNP: rs1058396 (GG) - Relevance:0.1
    Jk(a+/b-) kidd blood group, barring other variants
    SNP: rs58920878 (GG) - Relevance:0.1
    Slight (~2x) increase in colorectal cancer risk
    SNP: rs11881940 (TT) - Relevance:0.1
    1.9x risk of mi
    SNP: rs16990018 (AA) - Relevance:0.1
    Prp codon 171 asn - non-pathogenic variant
    SNP: rs9574 (CC) - Relevance:0.1
    Epcr h1 diplotype; reduced risk of vte?
    SNP: rs12469063 (GG) - Relevance:0.1
    Increased risk of developing restless legs syndrome
    SNP: rs7671167 (CC) - Relevance:0.1
    Chronic obstructive pulmonary disease
    SNP: rs17021918 (CT) - Relevance:0.1
    Prostate cancer
    SNP: rs2188962 (CT) - Relevance:0.1
    Crohn's disease
    SNP: rs1334710 (GG) - Relevance:0.1
    Increased risk
    SNP: rs7757037 (GA) - Relevance:0.1
    0.68x decreased risk for bipolar disorder
    SNP: rs548234 (TT) - Relevance:0.1
    Systemic lupus erythematosus
    SNP: rs9364554 (CC) - Relevance:0.1
    Prostate cancer
    SNP: rs1635852 (CC) - Relevance:0.1
    Height
    SNP: rs1334512 (GG) - Relevance:0.1
    0.37x decreased risk for severe malaria
    SNP: rs11556924 (TT) - Relevance:0.1
    Coronary heart disease
    SNP: rs9298506 (AA) - Relevance:0.1
    Higher risk aneurysm
    SNP: rs1412444 (TT) - Relevance:0.1
    Coronary heart disease
    SNP: rs3731566 (GG) - Relevance:0.1
    Higher bp if rs4961(t) carrier
    SNP: rs9525638 (TT) - Relevance:0.1
    Weaker bones
    SNP: rs9302752 (CC) - Relevance:0.1
    Leprosy
    SNP: rs17445836 (GG) - Relevance:0.1
    Multiple sclerosis
    SNP: rs885479 (GG) - Relevance:0.1
    Darker skin color
    SNP: rs8069176 (GG) - Relevance:0.1
    If 4 years old or younger, ~3x increased asthma risk if exposed to smoke
    SNP: rs3810291 (AA) - Relevance:0.1
    Body mass index
    SNP: rs17001266 (TT) - Relevance:0.1
    1.58x increased risk for schizophrenia in males
    SNP: rs1321172 (GG) - Relevance:0.1
    >1.08x risk
    SNP: rs11162922 (AA) - Relevance:0.1
    2x risk
    SNP: rs6680578 (TA) - Relevance:0.1
    1.11x risk
    SNP: rs11164838 (CC) - Relevance:0.1
    >1.11x risk
    SNP: rs6700998 (TT) - Relevance:0.1
    1.2x increased risk of atopic dermatitis.
    SNP: rs4845618 (GT) - Relevance:0.1
    1.7x increased melanoma risk
    SNP: rs4537545 (CC) - Relevance:0.1
    C-reactive protein
    SNP: rs28930069 (GG) - Relevance:0.1
    Hypokalemic periodic paralysis risk
    SNP: rs2291834 (CC) - Relevance:0.1
    Very slightly higher risk for myocardial infarction
    SNP: rs9282671 (AA) - Relevance:0.1
    Small chance of slightly increasing risk for a form of glaucoma
    SNP: rs2953145 (GC) - Relevance:0.1
    1.8x risk
    SNP: rs12487066 (CC) - Relevance:0.1
    >1.09x increased risk for multiple sclerosis
    SNP: rs9818870 (CC) - Relevance:0.1
    Coronary heart disease
    SNP: rs6807362 (CC) - Relevance:0.1
    Increased autism risk
    SNP: rs9851967 (TT) - Relevance:0.1
    0.88x risk of vitiligo in chinese
    SNP: rs28936383 (GG) - Relevance:0.1
    Limb-girdle muscular dystrophy-dystroglycanopathy
    SNP: rs6896702 (TT) - Relevance:0.1
    Increased risk of developing parkinson's disease
    SNP: rs17244841 (AA) - Relevance:0.1
    More responsive to statin treatment
    SNP: rs2544677 (GC) - Relevance:0.1
    1.3x risk of type-1 diabetes
    SNP: rs17166496 (CC) - Relevance:0.1
    1.1x risk for type-1 diabetes
    SNP: rs6897876 (CC) - Relevance:0.1
    Slight increase in testicular cancer risk for men
    SNP: rs13153971 (CC) - Relevance:0.1
    1.58x higher risk of asthma.
    SNP: rs9394492 (CC) - Relevance:0.1
    <0.76x risk for restless legs
    SNP: rs9387522 (AA) - Relevance:0.1
    Increased risk of cocaine induced paranoia.
    SNP: rs11983225 (TT) - Relevance:0.1
    7x less likely to respond to certain antidepressants
    SNP: rs445 (CC) - Relevance:0.1
    White blood cell types
    SNP: rs11767557 (TT) - Relevance:0.1
    Alzheimer's disease (late onset)
    SNP: rs9333649 (CC) - Relevance:0.1
    Associated with long qt syndrome
    SNP: rs6997709 (GG) - Relevance:0.1
    1.5x higher risk for hypertension
    SNP: rs1800546 (CC) - Relevance:0.1
    0.35x reduced risk of hereditary fructose intolerance.
    SNP: rs4979462 (TT) - Relevance:0.1
    Increased risk of developing primary biliary cirrhosis
    SNP: rs2283123 (CT) - Relevance:0.1
    Decreased risk of schizophrenia in limited study
    SNP: rs61735045 (AA) - Relevance:0.1
    Likely to be a benign variant
    SNP: rs12416000 (GG) - Relevance:0.1
    Homo sapiens gene (not neanderthal)
    SNP: rs911541 (GG) - Relevance:0.1
    1.48x increased risk of alzheimer's
    SNP: rs7078160 (GG) - Relevance:0.1
    Orofacial clefts
    SNP: rs3819331 (TT) - Relevance:0.1
    Lower risk of autism
    SNP: rs61749393 (CC) - Relevance:0.1
    Von willebrand disease, type 2b
    SNP: rs61749392 (CC) - Relevance:0.1
    Von willebrand disease, type 2b
    SNP: rs1805762 (CC) - Relevance:0.1
    >1.23x risk for hypertension
    SNP: rs9739493 (TC) - Relevance:0.1
    Higher risk for hypertension
    SNP: rs10492519 (AG) - Relevance:0.1
    Slightly increased risk of developing prostate cancer
    SNP: rs28940871 (GG) - Relevance:0.1
    23andme = tay-sachs disease likely, but on other platforms this may be the normal form
    SNP: rs2398162 (AA) - Relevance:0.1
    1.3x risk
    SNP: rs34516635 (GG) - Relevance:0.1
    Less longevity for ashkenazi jewish women.
    SNP: rs1344484 (TT) - Relevance:0.1
    1.5x risk
    SNP: rs16947078 (GG) - Relevance:0.1
    8x risk for allergic asthma
    SNP: rs736839 (CC) - Relevance:0.1
    Common, increased risk for sickle cell leg ulcers
    SNP: rs7250581 (GG) - Relevance:0.1
    1.4x risk
    SNP: rs11803731 (AA) - Relevance:0.1
    Straighter hair
    SNP: rs673548 (GA) - Relevance:0.1
    Metabolic syndrome
    SNP: rs6544713 (CC) - Relevance:0.1
    LDL cholesterol
    SNP: rs10201872 (CC) - Relevance:0.1
    Multiple sclerosis
    SNP: rs6050 (TT) - Relevance:0.1
    Fibrinogen
    SNP: rs4975616 (AA) - Relevance:0.1
    Lung cancer
    SNP: rs6905288 (GG) - Relevance:0.1
    Waist-hip ratio
    SNP: rs881858 (AA) - Relevance:0.1
    Chronic kidney disease
    SNP: rs1456893 (AA) - Relevance:0.1
    Crohn's disease
    SNP: rs11190140 (TC) - Relevance:0.1
    Crohn's disease
    SNP: rs381815 (CT) - Relevance:0.1
    Systolic blood pressure
    SNP: rs179247 (AA) - Relevance:0.1
    Slight increase (1.4x) in risk for graves disease
    SNP: rs7193343 (CC) - Relevance:0.1
    Atrial fibrillation
    SNP: rs7202877 (TT) - Relevance:0.1
    Type 1 diabetes
    SNP: rs1424233 (TC) - Relevance:0.1
    Obesity

  7. #2182
    Regular Member Achievements:
    Veteran25000 Experience PointsThree Friends
    Carlos's Avatar
    Join Date
    26-09-11
    Posts
    2,078
    Points
    30,981
    Level
    54
    Points: 30,981, Level: 54
    Level completed: 12%, Points required for next Level: 969
    Overall activity: 63.0%

    Y-DNA haplogroup
    E-V22>YF66572
    MtDNA haplogroup
    J1c5c1

    Ethnic group
    España
    Country: Spain



    Kit: Medieval Villa Magna Italy (R63)
    This sample really has a great lot of relevance.
    SNP: rs2290400 (TT) - Relevance:0.1
    Type 1 diabetes
    SNP: rs11672691 (GG) - Relevance:0.1
    1.39x increased risk for pcsm in patients with prostate cancer
    SNP: rs3748816 (AA) - Relevance:0.1
    Celiac disease
    SNP: rs7528419 (AA) - Relevance:0.1
    Lipoprotein-associated phospholipase A2 activity and mass
    SNP: rs7561317 (AG) - Relevance:0.1
    Weight
    SNP: rs2877716 (CC) - Relevance:0.1
    Two-hour glucose challenge
    SNP: rs12504628 (TT) - Relevance:0.1
    Pulmonary function
    SNP: rs2853677 (GG) - Relevance:0.1
    Lung adenocarcinoma
    SNP: rs4552569 (TT) - Relevance:0.1
    Ankylosing spondylitis
    SNP: rs2206734 (CC) - Relevance:0.1
    Body mass index
    SNP: rs3093024 (GG) - Relevance:0.1
    Rheumatoid arthritis
    SNP: rs301 (TT) - Relevance:0.1
    Metabolic syndrome (bivariate traits)
    SNP: rs1016343 (CC) - Relevance:0.1
    Prostate cancer
    SNP: rs17095355 (CC) - Relevance:0.1
    Biliary atresia
    SNP: rs6499640 (GA) - Relevance:0.1
    Weight
    SNP: rs9891119 (AA) - Relevance:0.1
    Multiple sclerosis
    SNP: rs6859 (AA) - Relevance:0.1
    Alzheimer's disease
    SNP: rs11581062 (GG) - Relevance:0.1
    Multiple sclerosis
    SNP: rs3126085 (GG) - Relevance:0.1
    Atopic dermatitis
    SNP: rs4085613 (GG) - Relevance:0.1
    Psoriasis
    SNP: rs7579899 (GG) - Relevance:0.1
    Renal cell carcinoma
    SNP: rs1420101 (CT) - Relevance:0.1
    Eosinophil counts
    SNP: rs2272127 (CC) - Relevance:0.1
    Associated with herpes and schizophrenia
    SNP: rs347685 (AA) - Relevance:0.1
    Chronic kidney disease
    SNP: rs734553 (GG) - Relevance:0.1
    Uric acid levels
    SNP: rs874040 (GG) - Relevance:0.1
    Rheumatoid arthritis
    SNP: rs1501908 (GC) - Relevance:0.1
    LDL cholesterol
    SNP: rs28936670 (GG) - Relevance:0.1
    Reversed normal
    SNP: rs3093023 (GG) - Relevance:0.1
    Rheumatoid arthritis
    SNP: rs4731702 (TT) - Relevance:0.1
    HDL cholesterol
    SNP: rs17582416 (TG) - Relevance:0.1
    Crohn's disease
    SNP: rs7395662 (GG) - Relevance:0.1
    HDL cholesterol
    SNP: rs1059513 (TT) - Relevance:0.1
    IgE levels
    SNP: rs12368653 (GG) - Relevance:0.1
    Multiple sclerosis
    SNP: rs4982731 (CC) - Relevance:0.1
    Possible higher risk of childhood acute lymphoblastic leukemia
    SNP: rs11636232 (CC) - Relevance:0.1
    Darker eye color
    SNP: rs7200786 (GG) - Relevance:0.1
    Multiple sclerosis
    SNP: rs9938149 (CC) - Relevance:0.1
    Central corneal thickness
    SNP: rs7238078 (TT) - Relevance:0.1
    Multiple sclerosis
    SNP: rs1077667 (CC) - Relevance:0.1
    Multiple sclerosis
    SNP: rs8102137 (CC) - Relevance:0.1
    Bladder cancer
    SNP: rs6088813 (CC) - Relevance:0.1
    Height
    SNP: rs1012068 (TT) - Relevance:0.1
    Chronic Hepatitis C infection
    SNP: rs864537 (AA) - Relevance:0.1
    Celiac disease and Rheumatoid arthritis
    SNP: rs1427407 (GG) - Relevance:0.1
    F-cell distribution
    SNP: rs9834970 (TC) - Relevance:0.1
    Bipolar disorder
    SNP: rs4635969 (GG) - Relevance:0.1
    Testicular germ cell cancer
    SNP: rs3806932 (GG) - Relevance:0.1
    Eosinophilic esophagitis (pediatric)
    SNP: rs11984041 (CC) - Relevance:0.1
    Stroke
    SNP: rs7805747 (GG) - Relevance:0.1
    Chronic kidney disease
    SNP: rs1015213 (CC) - Relevance:0.1
    Glaucoma (primary open-angle)
    SNP: rs3793917 (CC) - Relevance:0.1
    Age-related macular degeneration
    SNP: rs1021188 (TT) - Relevance:0.1
    Bone mineral density
    SNP: rs3894194 (AA) - Relevance:0.1
    Asthma
    SNP: rs4648356 (CC) - Relevance:0.1
    Multiple sclerosis
    SNP: rs4660293 (AA) - Relevance:0.1
    HDL cholesterol
    SNP: rs560426 (TT) - Relevance:0.1
    Orofacial clefts
    SNP: rs1335532 (AA) - Relevance:0.1
    Multiple sclerosis
    SNP: rs2274910 (CC) - Relevance:0.1
    Crohn's disease
    SNP: rs1011731 (GG) - Relevance:0.1
    Waist-hip ratio
    SNP: rs9286879 (AA) - Relevance:0.1
    Crohn's disease
    SNP: rs2786098 (GG) - Relevance:0.1
    Asthma
    SNP: rs28937591 (GG) - Relevance:0.1
    Deafness expected
    SNP: rs6732426 (CC) - Relevance:0.1
    Curlier hair
    SNP: rs12478601 (CC) - Relevance:0.1
    Polycystic ovary syndrome
    SNP: rs7595037 (CT) - Relevance:0.1
    Multiple sclerosis
    SNP: rs1007371 (TT) - Relevance:0.1
    Rare genotype.
    SNP: rs6710518 (TT) - Relevance:0.1
    Bone mineral density
    SNP: rs7578326 (AG) - Relevance:0.1
    Type 2 diabetes
    SNP: rs10934853 (CC) - Relevance:0.1
    Prostate cancer

  8. #2183
    Regular Member Achievements:
    Veteran25000 Experience PointsThree Friends
    Carlos's Avatar
    Join Date
    26-09-11
    Posts
    2,078
    Points
    30,981
    Level
    54
    Points: 30,981, Level: 54
    Level completed: 12%, Points required for next Level: 969
    Overall activity: 63.0%

    Y-DNA haplogroup
    E-V22>YF66572
    MtDNA haplogroup
    J1c5c1

    Ethnic group
    España
    Country: Spain



    Kit: Medieval Villa Magna Italy (R63)

    SNP: rs3796619 (AA) - Relevance:0.1
    Recombination rate (males)
    SNP: rs2082412 (AA) - Relevance:0.1
    Psoriasis
    SNP: rs2731672 (CC) - Relevance:0.1
    Activated partial thromboplastin time
    SNP: rs11755527 (CC) - Relevance:0.1
    Type 1 diabetes
    SNP: rs1055144 (CC) - Relevance:0.1
    Waist-hip ratio
    SNP: rs730497 (GG) - Relevance:0.1
    Glycated hemoglobin levels
    SNP: rs2282978 (CC) - Relevance:0.1
    Height
    SNP: rs1454292 (CC) - Relevance:0.1
    Curlier hair
    SNP: rs4410871 (CC) - Relevance:0.1
    Multiple sclerosis
    SNP: rs1913517 (AA) - Relevance:0.1
    Systemic lupus erythematosus
    SNP: rs11228565 (GG) - Relevance:0.1
    Prostate cancer
    SNP: rs614367 (CC) - Relevance:0.1
    Breast cancer
    SNP: rs7396835 (CC) - Relevance:0.1
    Quantitative traits
    SNP: rs4238010 (GG) - Relevance:0.1
    Highly correlated risk factor for major depressive disorder.
    SNP: rs2650000 (CC) - Relevance:0.1
    Metabolic traits
    SNP: rs626277 (AA) - Relevance:0.1
    Chronic kidney disease
    SNP: rs4788084 (CC) - Relevance:0.1
    Type 1 diabetes
    SNP: rs28937908 (TT) - Relevance:0.1
    No call
    SNP: rs280519 (GG) - Relevance:0.1
    Psoriasis
    SNP: rs11538758 (CC) - Relevance:0.1
    Prp codon p105 - non-pathogenic form
    SNP: rs28933385 (GG) - Relevance:0.1
    Prion protein codon 200 (e) - non pathogenic variant
    SNP: rs6102059 (CC) - Relevance:0.1
    LDL cholesterol
    SNP: rs2828520 (GG) - Relevance:0.1
    1.35x major depressive disorder risk



  9. #2184
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    Y-DNA haplogroup
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    1 members found this post helpful.
    “If you ain't first you're last” (Ricky Bobby)

    ... from the North Roman Warrior to the Minoan ...













  10. #2185
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    2 members found this post helpful.
    Quote Originally Posted by Salento View Post
    You are the #1 top match to this sample! :)

    You are #1 among 895 other users who also have a deep dive match with this sample. This makes your relationship to this individual very unique. Full research for this sample is activated for you regardless of your access level ...

    You always get the glory

    I only have

    Late Medieval Villa Magna Italy


    1355 AD


    R52





    mtDNA: T1a1Y-DNA: G-PF3239

    You are the #2 top match to this sample!



    My paternal grandfather was mtdna T1a1e



    and this below


    Illyrian / Dalmatian


    1600 BC


    I4331





    mtDNA: I1a1Y-DNA: J2b2a

    You are a top 99% match to this sample! This makes your relationship to this individual exceptional.


    and lastly



    Central Roman

    590 AD

    SZ32



    mtDNA: H74 ?

    You are a top 99% match to this sample! This makes your relationship to this individual exceptional.
    Fathers mtdna T2b17
    Grandfather mtdna T1a1e
    Sons mtdna K1a4o
    Mum paternal line R1b-S8172
    Grandmum paternal side I1d1-P109
    Wife paternal line R1a-Z282

  11. #2186
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    1 members found this post helpful.
    Quote Originally Posted by torzio View Post
    You always get the glory

    I only have

    Late Medieval Villa Magna Italy


    1355 AD


    R52





    mtDNA: T1a1Y-DNA: G-PF3239

    You are the #2 top match to this sample!



    My paternal grandfather was mtdna T1a1e



    and this below


    Illyrian / Dalmatian


    1600 BC


    I4331





    mtDNA: I1a1Y-DNA: J2b2a

    You are a top 99% match to this sample! This makes your relationship to this individual exceptional.


    and lastly



    Central Roman


    590 AD


    SZ32





    mtDNA: H74 ?

    You are a top 99% match to this sample! This makes your relationship to this individual exceptional.
    congrats:)

    There’s obviously a hierarchy difference between SNPs chain and Distance,
    they don't necessarily go together.

    some more:















  12. #2187
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    North Italian
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    1 members found this post helpful.
    Quote Originally Posted by Salento View Post
    congrats:)

    There’s obviously a hierarchy difference between SNPs chain and Distance,
    they don't necessarily go together.

    some more:















    what I presented is all I have for me on MTA

  13. #2188
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    MtDNA haplogroup
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    It’s important to interpret some of the SNPs chains.

    in my case:

    it’s possible that the North Roman Warrior carries some of my Southern European DNA, and that I carry some in common Ancient DNA with a Minoan.

    That doesn’t make me a Gaul or a Minoan,

    I just have an old genetic relation, and that’s it :)

  14. #2189
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    Y-DNA haplogroup
    T1a2 -Z19945
    MtDNA haplogroup
    H12a

    Ethnic group
    Italian
    Country: United States



    1 members found this post helpful.
    Edit ...
    deep dive map




    1. Hellenic Roman Monterotondo (165 AD) ..... 10.39 - R1548 -
    Top
    98
    % match vs all users


    2. Tuscan Medieval Cancelleria Basilica (1350 AD) ..... 10.88 - R1290 -
    Top
    98
    % match vs all users


    3. Imperial Rome Empire Via Paisiello (100 AD) ..... 11.19 - R114 -
    Top
    98
    % match vs all users


    4. Imperial Rome Centocelle (200 AD) ..... 11.31 - R49 -
    Top
    99
    % match vs all users


    5. Central Roman (590 AD) ..... 11.62 - SZ36 -
    Top
    97
    % match vs all users


    6. Tuscan Late Medieval Villa Magna Italy (1355 AD) ..... 11.81 - R56 -
    Top
    99
    % match vs all users


    7. Hellenic Roman (590 AD) ..... 11.97 - SZ40 - ?
    Top
    97
    % match vs all users


    8. Medieval Villa Magna Italy (1100 AD) ..... 11.97 - R58 -
    Top
    99
    % match vs all users


    9. Late Roman Empire Crypta Balbi (500 AD) ..... 12.03 - R107 -
    Top
    98
    % match vs all users


    10. Hellenic Roman Casale del Dolce (145 AD) ..... 12.04 - R123 -
    Top
    98
    % match vs all users


    11. Hellenic Roman Marcellino (400 AD) ..... 12.08 - R136-
    Top
    97
    % match vs all users


    12. Tuscan Medieval Villa Magna Italy (905 AD) ..... 12.3 - R60 -
    Top
    97
    % match vs all users


    13. Central Roman San Ercolano (100 AD) ..... 12.42 - R117 -
    Top
    98
    % match vs all users


    14. Central Roman (580 AD) ..... 12.48 - CL121 -
    Top
    97
    % match vs all users


    15. Hellenic Roman ANAS (200 AD) ..... 12.53 - R73 -
    Top
    97
    % match vs all users


    16. Central Roman / Mixed (590 AD) ..... 12.57 - SZ19 -
    Top
    98
    % match vs all users


    17. Torna Alta Andalusia (1550 AD) ..... 12.69 - I3808 -
    Top
    99
    % match vs all users


    18. Medieval Villa Magna Italy (1100 AD) ..... 12.87 - R65 -
    Top
    97
    % match vs all users


    19. Imperial Rome Centocelle (190 AD) ..... 13.01 - R50 -
    Top
    98
    % match vs all users


    20. Central Roman Mausoleo Augusto (500 AD) ..... 13.12- R30 -
    Top
    98
    % match vs all users
    Last edited by Salento; 19-01-20 at 13:13.

  15. #2190
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    E-V22>YF66572
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    J1c5c1

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    2 members found this post helpful.
















  16. #2191
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    Y-DNA haplogroup
    R1b-DF27-FGC35133

    Ethnic group
    Portuguese-Brazilian
    Country: Brazil



    3 members found this post helpful.
    I have excepcional and unique relationship with two individuals. I do not had see this. Cool.





  17. #2192
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    1 members found this post helpful.
    Duarte I also have Illercavones. Who was going to tell me when the first time and the only one I was and the state in Lleida I was there on the stage of the Principal Theater of Lleida at the premiere of a movie where I had a small role, the truth is that via the people much prettier than layetanos. Cogotas already knew it and I knew it because I said long ago that a brother of my maternal grandfather carved some bulls in wood and they are nailed to Guisando's bulls. The iberian settlemen as the town where I live already gives me an attack, I have asked but they have not answered me yet.

  18. #2193
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    Y-DNA haplogroup
    R1b-BY3449
    MtDNA haplogroup
    H1e1a

    Ethnic group
    Italian and Iberian
    Country: Brazil



    1 members found this post helpful.
    Quote Originally Posted by Duarte View Post
    I have excepcional and unique relationship with two individuals. I do not had see this. Cool.
    I have with one! NOICE!


  19. #2194
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    Y-DNA haplogroup
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    Ethnic group
    Celto-Germanic
    Country: USA - Rhode Island



    1 members found this post helpful.
    I am #1 match to Trumpington Meadows Bronze Age in England!

  20. #2195
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    Quote Originally Posted by Joey37 View Post
    I am #1 match to Trumpington Meadows Bronze Age in England!
    The old kits that I created from Iberia de El Argar, La loma del puerco, Cogotas, ilergetes, e.t.c selected Trumpington or what it means that Trumpington would get them.

  21. #2196
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    3 members found this post helpful.
    Nice, guys. :)

    Only two show up and I don't completely understand either one, but I'll give it my best shot.





    I quite understand that in terms of modern populations, both of these ancient samples plot somewhere near Toscana. The question is "why"?

    We don't really know anything about the Crete Armenoi sample other than to say it's not from the Minoan period but rather later, and she's an outlier as far as Minoans are concerned.

    As for Scythian Moldova, why a "Tuscan" like individual is a member of an Iron Age pastoral group with origins on the steppes I don't know. Perhaps it's a similar situation to that in Iron Age Thrace, where there were "Tuscan like", broadly speaking, individuals, and also in late Empire/Early Medieval Antiquity, along with some more northwestern leaning Tuscans.

    Is it that there were still populations much like those on the northern part of the Italian peninsula spread all over Central Europe, the Balkans, and even into Moldova?

    From the paper...

    " Between 700 and 300 BCE, the Scythians, representing mobile pastoral nomads of a new militaristic type (1), dominated the Pontic-Kazakh steppe, occupying an area from the Altai to the Carpathian Mountains. Their decline began around 300 BCE and was caused by intensifying hostile relations with the Macedonians in the West and the invasion of the Sarmatians from the East. The Sarmatians and the Scythians are thought to have coexisted for a few centuries, but eventually, the former group prevailed (2), resulting in the Scythian downfall. The Sarmatians are believed to comprise a number of groups of similar nomadic background (8), and they became the politically most influential force within the eastern fringes of the Roman Empire at the time. Their decline (~400 CE) was associated with the attack of the Goths and the subsequent invasion of the Huns (8)."

    "
    The Scythians reported in this study, from the core Scythian territory in the North Pontic steppe (12), showed high intragroup diversity. In the PCA, they are positioned as four visually distinct groups compared to the gradient of present-day populations (Fig. 1C): (i) A group of three individuals (scy009, scy010, and scy303) showed genetic affinity to north European populations, hereafter referred to as a north European (NE) cluster. (ii) A group of four individuals (scy192, scy197, scy300, and scy305) showed genetic similarities to southern European populations, hereafter referred to as a south European (SE) cluster. (iii) A group of three individuals (scy006, scy011, and scy193) located between the genetic variation of Mordovians and populations of the North Caucasus, hereafter referred to as a steppe cluster (SC). In addition, one Srubnaya-Alakulskaya individual (kzb004), the most recent Cimmerian (cim357), and all Sarmatians fell within this cluster."

    "
    Scythians belonging to the SE cluster were closer to Hungarian Bronze Age and Iron Age individuals including Vatya and Maros. " This doesn't at all surprise me. Other studies have shown the tie between Italians (and I) and the Hungarian Bronze Age and Maros as well.

    "
    Some of the Scythians of the western Pontic-Caspian steppe lacked the SA and the East Eurasian components altogether and instead were more similar to a Montenegro Iron Age individual (3), possibly indicating assimilation of the earlier local groups by the Scythians. "

    https://advances.sciencemag.org/content/4/10/eaat4457



    Non si fa il proprio dovere perchè qualcuno ci dica grazie, lo si fa per principio, per se stessi, per la propria dignità. Oriana Fallaci

  22. #2197
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    Y-DNA haplogroup
    R1b-U152-Z56-BY3957
    MtDNA haplogroup
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    15/32 British, 5/32 German, 9/64 Irish, 1/8 Scots Gaelic, 5/64 French, 1/32 Welsh
    Country: USA - Washington



    1 members found this post helpful.
    Wouldnt it be cool if the Moderators made a map; based on MyTrueAncestry samples?
    It would be awesome to compare how accurate Tacitus and Livy was. : D
    Here is my Admixture.
    28% Celt

    72% Germanic

    22.5% Danish Viking
    14.5% Frankish
    8.5% Suebi
    8.5% Saxon
    12.5% Viking (6.5% Norseman, 6% Swedes)
    5.5% East Germanic (2% Visigoth, 2% Vandal, 1.5% Ostrogoth)

  23. #2198
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    E-V22>YF66572
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    España
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    Now that I am looking for my father in a simile like a stolen child and I will not stop until I get it. I know that everything is autosomal but it must also be there somewhere. So I had already noticed this sample and I will create the kit.



    I have seen something and it has several Deep Dive from Egypt and Cluana Ancona and more... I have to go to the blog all the files and then publish them here, web of work.

  24. #2199
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    Y-DNA haplogroup
    R1B U106 L44
    MtDNA haplogroup
    A2

    Ethnic group
    Mixed , mostly Italian
    Country: Uruguay



    Mine....


    Hispano-Roman Taifa of Valencia
    1200 AD
    I12647
    mtDNA: H1ak1
    You are a top 96% match to this sample! This makes your relationship to this individual exceptional.
    Shared DNA: (Sample Quality: 33)
    3 SNP chains (min. 60 SNPs) / 17.72 cM
    Largest segment=158 SNPs / 7.59 cM

    Your raw DNA is 96% closer than other matching users

    Iberian Cordoba Caliphate
    1050 AD
    I7498
    mtDNA: H3a1Y-DNA: E1b1b1a1b1a
    You are a top 98% match to this sample! This makes your relationship to this individual exceptional.
    Shared DNA: (Sample Quality: 34)
    3 SNP chains (min. 60 SNPs) / 12.24 cM
    Largest segment=287 SNPs / 6.06 cM

    Your raw DNA is 98% closer than other matching users


    Ostrogoth Mix
    495 AD
    AEH_1
    mtDNA: H5 ?
    You are a top 97% match to this sample! This makes your relationship to this individual exceptional.
    Shared DNA: (Sample Quality: 8)
    2 SNP chains (min. 60 SNPs) / 4.9 cM
    Largest segment=376 SNPs / 2.81 cM

    Your raw DNA is 97% closer than other matching users

  25. #2200
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    E-V22>YF66572
    MtDNA haplogroup
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    Ethnic group
    España
    Country: Spain



    1 members found this post helpful.


    1. Spanish_Cataluna (7.155)
    2. Spanish_Murcia (7.269)
    3. Spanish_Castilla_Y_Leon (7.528)
    4. Spanish_Valencia (7.691)
    5. Portuguese (8.220)
    6. Spanish_Extremadura (8.433)
    7. Spanish_Andalucia (8.449)
    8. Spanish_Castilla_La_Mancha (8.936)





    1. Spanish_Aragon (5.017)
    2. Spanish_Valencia (6.046)
    3. Spanish_Castilla_La_Mancha (6.695)
    4. Spanish_Andalucia (7.904)
    5. Southwest_French (8.076)
    6. Spanish_Cantabria (8.328)
    7. Spanish_Murcia (8.987)
    8. Spanish_Castilla_Y_Leon (9.225)



    These two men are classified in MTA as Roman culture.


    These samples of who could be treated?

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