WickedWise
Junior Member
- Messages
- 2
- Reaction score
- 1
- Points
- 0
- Location
- California
- Ethnic group
- German, Irish, English, Russian, Polish, Austrian, Romanian, AJ, Canadian, Hungarian, Czech, etc
- mtDNA haplogroup
- H4a1a1a
I just received my 23andMe results as well and I am H4a. I live in the US and my mother was adopted so I know very little on her side. My results came back as:
99.5% European
50.2% Ashkenazi Jewish
34.2% NW European - 22.6% Scandinavian, 5.5% British & Irish, 6.2% Broadly European
10.5% Eastern European
0.3% Southern European - 0.3% Broadly S. European
4.3% Broadly European
0.5% East Asian & Native American
<0.1% Sub-Saharan African
MtDNA H4a
I don't talk to my father and all my grandparents have passed away but of course I can only assume the same of my mothers birth parents.
I'm just pretty much digging around looking for information to expand what I have found.
I do know that the genetic disease gene, Alpha-1 Antitrypsin Deficiency, that I carry (MZ) most likely came from my mother's Scandinavian side. It was originally most prevalent there. I also have Leri's Disease/Melorheostosis in my foot but due to its rarity they haven't made any genetic connections although many sufferers have multiple family members with it.
So, I suppose that is my story.
I'm glad to have found a bit of information here and I hope we find more as a team!
99.5% European
50.2% Ashkenazi Jewish
34.2% NW European - 22.6% Scandinavian, 5.5% British & Irish, 6.2% Broadly European
10.5% Eastern European
0.3% Southern European - 0.3% Broadly S. European
4.3% Broadly European
0.5% East Asian & Native American
<0.1% Sub-Saharan African
MtDNA H4a
I don't talk to my father and all my grandparents have passed away but of course I can only assume the same of my mothers birth parents.
I'm just pretty much digging around looking for information to expand what I have found.
I do know that the genetic disease gene, Alpha-1 Antitrypsin Deficiency, that I carry (MZ) most likely came from my mother's Scandinavian side. It was originally most prevalent there. I also have Leri's Disease/Melorheostosis in my foot but due to its rarity they haven't made any genetic connections although many sufferers have multiple family members with it.
So, I suppose that is my story.
I'm glad to have found a bit of information here and I hope we find more as a team!