rs9494266
A SNP in the C6orf217 gene on chromosome 6. Its most notable genotype is G;G.
- Gene
- C6orf217
- Location
- Chr 6135,530,435 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 24%
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 57%
- European ancestry (Utah)G;G 86%
- Han Chinese (Beijing)G;G 84%
- Japanese (Tokyo)G;G 88%
- Yoruba (Nigeria)G;G 5%
- African ancestry (Southwest US)G;G 18%
- Chinese (Denver)G;G 84%
- Gujarati IndianG;G 77%
- Luhya (Kenya)G;G 7%
- Mexican ancestry (Los Angeles)G;G 76%
- Maasai (Kenya)G;G 10%
- TuscanG;G 91%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
Originally reported to be associated with type-2 diabetes in a genome-wide association study; yet then reported not to be associated with either T2D or related metabolic traits in a large Danish population (ultimately 17,000 patients for the latter study).
Source and license
Adapted from rs9494266 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.