rs12571093
A SNP in the LOC100128041 gene on chromosome 10. Its most notable genotype is A;A: ancestral Neanderthal allele (homozygote)
- Gene
- LOC100128041
- Location
- Chr 1068,259,614 (GRCh38)
- Highest magnitude
- 1.0Minor
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 13%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableNot ratedancestral Neanderthal allele (homozygote)
- A;GNot ratedancestral Neanderthal allele (heterozygote)
- G;GGoodcommon on affy axiom data
On SNPedia: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 10 HapMap populations.
- AverageA;A 2% A;G 20% G;G 78%
- European ancestry (Utah)A;A 2% A;G 20% G;G 78%
- Han Chinese (Beijing)A;A 4% A;G 26% G;G 69%
- Japanese (Tokyo)A;A 2% A;G 21% G;G 77%
- Yoruba (Nigeria)A;A 0% A;G 0% G;G 100%
- African ancestry (Southwest US)A;A 0% A;G 7% G;G 93%
- Chinese (Denver)A;A 3% A;G 28% G;G 69%
- Gujarati IndianA;A 5% A;G 34% G;G 61%
- Mexican ancestry (Los Angeles)A;A 0% A;G 41% G;G 59%
- Maasai (Kenya)A;A 0% A;G 6% G;G 94%
- TuscanA;A 3% A;G 21% G;G 77%
Source and license
Adapted from rs12571093 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.