rs539901
A SNP in the LOC101928635 gene on chromosome 15. Its most notable genotype is T;T: common genotype
- Gene
- LOC101928635
- Location
- Chr 1558,382,470 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- AncestryDNA
- Minor allele frequency
- 6%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (T;T). 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.
- AverageT;T 85%
- European ancestry (Utah)T;T 97%
- Han Chinese (Beijing)T;T 81%
- Japanese (Tokyo)T;T 84%
- Yoruba (Nigeria)T;T 74%
- African ancestry (Southwest US)T;T 88%
- Chinese (Denver)T;T 74%
- Gujarati IndianT;T 91%
- Luhya (Kenya)T;T 70%
- Mexican ancestry (Los Angeles)T;T 91%
- Maasai (Kenya)T;T 83%
- TuscanT;T 97%
Related
Other LOC101928635 SNPs
- rs493258C;T1.15x risk of Age Related Macular DegenerationWorth knowing
- rs10468017C;Tassociated with higher HDL cholesterolWorth knowing
- rs1800588C;Thigher HDL-C levelsMinor
- rs2414539A;Acommon in complete genomicsTypical
- rs4775041C;Clowest phosphatidylethanolamine valuesTypical
- rs16939881G;Gcommon genotypeTypical
- rs16940212G;Gcommon in complete genomicsTypical
Source and license
Adapted from rs539901 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.