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.

  1. G;GMost notableBad>1.95x increased risk of Crohn's disease in JapaneseTypical · 0.01% of people
  2. G;TBad1.95x increased risk of Crohn's disease in JapaneseTypical · 0.017% of people
  3. T;TGoodNo summary available.Typical · 0.082% of people

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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.