rs10995356
A SNP in the LOC107984012 gene on chromosome 10. Its most notable genotype is A;A: Likely more reward dependent
- Gene
- LOC107984012
- Location
- Chr 1062,896,153 (GRCh38)
- Highest magnitude
- 1.5Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 33%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableNot ratedLikely more reward dependent
- A;GNot ratedNo tendency in either direction
- G;GNot ratedLikely less reward dependent
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 12% A;G 34% G;G 54%
- European ancestry (Utah)A;A 26% A;G 42% G;G 33%
- Han Chinese (Beijing)A;A 12% A;G 40% G;G 48%
- Japanese (Tokyo)A;A 10% A;G 41% G;G 50%
- Yoruba (Nigeria)A;A <1% A;G 10% G;G 90%
- African ancestry (Southwest US)A;A 0% A;G 26% G;G 74%
- Chinese (Denver)A;A 8% A;G 51% G;G 40%
- Gujarati IndianA;A 27% A;G 51% G;G 23%
- Luhya (Kenya)A;A 0% A;G 5% G;G 96%
- Mexican ancestry (Los Angeles)A;A 28% A;G 48% G;G 24%
- Maasai (Kenya)A;A 2% A;G 16% G;G 82%
- TuscanA;A 19% A;G 47% G;G 34%
Source and license
Adapted from rs10995356 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.