rs1360517
A SNP in the LOC107987047 gene on chromosome 9. Its most notable genotype is C;T: Higher susceptibility for AIDS
- Gene
- LOC107987047
- Location
- Chr 913,007,130 (GRCh38)
- Highest magnitude
- 1.5Minor
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 11%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs1360517 on the minus strand: (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.
- AverageC;T 24% C;C 73%
- European ancestry (Utah)C;T 19% C;C 81%
- Han Chinese (Beijing)C;T 22% C;C 77%
- Japanese (Tokyo)C;T 13% C;C 86%
- Yoruba (Nigeria)C;T 32% C;C 64%
- African ancestry (Southwest US)C;T 23% C;C 77%
- Chinese (Denver)C;T 25% C;C 74%
- Gujarati IndianC;T 27% C;C 66%
- Luhya (Kenya)C;T 30% C;C 63%
- Mexican ancestry (Los Angeles)C;T 5% C;C 95%
- Maasai (Kenya)C;T 37% C;C 54%
- TuscanC;T 29% C;C 70%
Source and license
Adapted from rs1360517 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.