rs3763305
A SNP in the LOC101929163 gene on chromosome 6. Its most notable genotype is G;G: common in complete genomics
- Gene
- LOC101929163
- Location
- Chr 632,401,711 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 6%
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 9 HapMap populations.
- AverageG;G 89%
- European ancestry (Utah)G;G 82%
- Han Chinese (Beijing)G;G 91%
- Japanese (Tokyo)G;G 88%
- Yoruba (Nigeria)G;G 100%
- African ancestry (Southwest US)G;G 97%
- Chinese (Denver)G;G 90%
- Gujarati IndianG;G 92%
- Mexican ancestry (Los Angeles)G;G 66%
- TuscanG;G 94%
Related
Other LOC101929163 SNPs
- rs3129934T;T3.3x increased risk for multiple sclerosisWorth knowing
- rs498422G;G>1.42x slightly higher risk for infertility in Chinese menMinor
- rs10947262C;C1.3x increased risk for osteoarthritisMinor
- rs1980493T;Tcommon on affy axiom dataTypical
- rs2076530T;T2x risk for sarcoidosisTypical
- rs2395148G;Gcommon in complete genomicsTypical
- rs3117103A;Acommon on affy axiom dataTypical
- rs3130340T;TNo summary available.Typical
Source and license
Adapted from rs3763305 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.