rs10486776
A SNP in the LOC101927558 gene on chromosome 7. Its most notable genotype is G;G: common on affy axiom data
- Gene
- LOC101927558
- Location
- Chr 715,703,161 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 8%
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 10 HapMap populations.
- AverageG;G 84%
- European ancestry (Utah)G;G 89%
- Han Chinese (Beijing)G;G 70%
- Japanese (Tokyo)G;G 86%
- Yoruba (Nigeria)G;G 96%
- Chinese (Denver)G;G 69%
- Gujarati IndianG;G 81%
- Luhya (Kenya)G;G 95%
- Mexican ancestry (Los Angeles)G;G 90%
- Maasai (Kenya)G;G 94%
- TuscanG;G 66%
Notes
From SNPedia
Notes
Confirmation of genomewide association signals in Chinese Han population reveals risk loci for ischemic stroke.
Source and license
Adapted from rs10486776 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.