rs8179116
A SNP in the LOC105369968 gene on chromosome 12. Its most notable genotype is C;C: common in complete genomics
- Gene
- LOC105369968
- Location
- Chr 12108,631,651 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 2%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs8179116 on the minus strand: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 6 HapMap populations.
- AverageC;C 91%
- European ancestry (Utah)C;C 99%
- Japanese (Tokyo)C;C 99%
- Yoruba (Nigeria)C;C 82%
- African ancestry (Southwest US)C;C 84%
- Luhya (Kenya)C;C 85%
- Maasai (Kenya)C;C 96%
Source and license
Adapted from rs8179116 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.