rs12416000
A SNP on chromosome 10. Its most notable genotype is A;A: Neanderthal gene
- Gene
- None listed
- Location
- Chr 104,797,975 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 11%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableNot ratedNeanderthal gene
- A;GNot ratedmixed homo-sapiens (human) and Neanderthal
- G;GNot ratedhomo sapiens gene (not Neanderthal)
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 11 HapMap populations.
- AverageA;A 2% A;G 19% G;G 79%
- European ancestry (Utah)A;A 2% A;G 20% G;G 79%
- Han Chinese (Beijing)A;A 3% A;G 26% G;G 72%
- Japanese (Tokyo)A;A 4% A;G 24% G;G 72%
- 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 30% G;G 67%
- Gujarati IndianA;A 2% A;G 36% G;G 62%
- Luhya (Kenya)A;A 0% A;G 7% G;G 93%
- Mexican ancestry (Los Angeles)A;A 2% A;G 33% G;G 66%
- Maasai (Kenya)A;A 1% A;G 15% G;G 84%
- TuscanA;A 2% A;G 14% G;G 84%
Notes
From SNPedia
Notes
G;G
This is the human, homo sapiens version of the gene, not the neanderthal version.
Source and license
Adapted from rs12416000 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.