rs1359645
A SNP in the LOC102724439 gene on chromosome 10. Its most notable genotype is A;A: common in complete genomics
- Gene
- LOC102724439
- Location
- Chr 10106,285,899 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 15%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 10 HapMap populations.
- AverageA;A 61%
- European ancestry (Utah)A;A 96%
- Han Chinese (Beijing)A;A 71%
- Japanese (Tokyo)A;A 55%
- Yoruba (Nigeria)A;A 37%
- African ancestry (Southwest US)A;A 53%
- Chinese (Denver)A;A 57%
- Gujarati IndianA;A 55%
- Luhya (Kenya)A;A 51%
- Maasai (Kenya)A;A 42%
- TuscanA;A 95%
Source and license
Adapted from rs1359645 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.