rs7765379
A SNP on chromosome 6. Its most notable genotype is G;G: >1.95x increased risk of Crohn's disease in Japanese
- Gene
- None listed
- Location
- Chr 632,713,151 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 12%
Genotypes
As shown in 23andMe and AncestryDNA files.
- G;GMost notableBad>1.95x increased risk of Crohn's disease in Japanese
- G;TBad1.95x increased risk of Crohn's disease in Japanese
- T;TGoodNo summary available.
On SNPedia: (G;G), (G;T), (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.
- AverageG;G 1% G;T 17% T;T 82%
- European ancestry (Utah)G;G 0% G;T 19% T;T 81%
- Han Chinese (Beijing)G;G <1% G;T 17% T;T 83%
- Japanese (Tokyo)G;G 3% G;T 29% T;T 68%
- Yoruba (Nigeria)G;G 1% G;T 18% T;T 81%
- African ancestry (Southwest US)G;G 2% G;T 14% T;T 84%
- Chinese (Denver)G;G <1% G;T 8% T;T 91%
- Gujarati IndianG;G 0% G;T 9% T;T 91%
- Luhya (Kenya)G;G 0% G;T 16% T;T 84%
- Mexican ancestry (Los Angeles)G;G 2% G;T 21% T;T 77%
- Maasai (Kenya)G;G 2% G;T 15% T;T 83%
- TuscanG;G 0% G;T 24% T;T 76%
Source and license
Adapted from rs7765379 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.