rs332951
A SNP in the LOC105377896 gene on chromosome 6. Its most notable genotype is C;C.
- Gene
- LOC105377896
- Location
- Chr 692,597,090 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 3%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 9 HapMap populations.
- AverageC;C 91%
- European ancestry (Utah)C;C 86%
- Han Chinese (Beijing)C;C 91%
- Japanese (Tokyo)C;C 80%
- Yoruba (Nigeria)C;C 96%
- African ancestry (Southwest US)C;C 98%
- Gujarati IndianC;C 79%
- Luhya (Kenya)C;C 95%
- Maasai (Kenya)C;C 98%
- TuscanC;C 93%
Related
Notes
From SNPedia
Notes
Rs332951 is an intergenic SNP, located most closely to the genes EPHA7 (642932 bps) and MIR4643 (1075353 bp). Based on the draft Neanderthal genome () it is thought the T allele of this SNP may be derived from Neanderthal admixture.
Source and license
Adapted from rs332951 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.