rs16940212
A SNP in the LOC101928635 gene on chromosome 15. Its most notable genotype is G;G: common in complete genomics
- Gene
- LOC101928635
- Location
- Chr 1558,401,821 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 18%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (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.
- AverageG;G 71%
- European ancestry (Utah)G;G 63%
- Han Chinese (Beijing)G;G 55%
- Japanese (Tokyo)G;G 42%
- Yoruba (Nigeria)G;G 89%
- African ancestry (Southwest US)G;G 90%
- Chinese (Denver)G;G 57%
- Gujarati IndianG;G 69%
- Luhya (Kenya)G;G 86%
- Mexican ancestry (Los Angeles)G;G 86%
- Maasai (Kenya)G;G 84%
- TuscanG;G 64%
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
- rs539901T;Tcommon genotypeTypical
- rs2414539A;Acommon in complete genomicsTypical
- rs4775041C;Clowest phosphatidylethanolamine valuesTypical
- rs16939881G;Gcommon genotypeTypical
Source and license
Adapted from rs16940212 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.