rs2305767

A SNP in the MYO9B gene on chromosome 19. Its most notable genotype is T;T: common/normal

Gene
MYO9B
Location
Chr 1917,183,487 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
25%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon/normalTypical · 0.065% of people

SNPedia records rs2305767 on the minus strand: (A;A). 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.

  • AverageT;T 65%
  • European ancestry (Utah)T;T 35%
  • Han Chinese (Beijing)T;T 58%
  • Japanese (Tokyo)T;T 62%
  • Yoruba (Nigeria)T;T 99%
  • African ancestry (Southwest US)T;T 86%
  • Chinese (Denver)T;T 58%
  • Gujarati IndianT;T 39%
  • Luhya (Kenya)T;T 96%
  • Mexican ancestry (Los Angeles)T;T 64%
  • Maasai (Kenya)T;T 89%
  • TuscanT;T 35%

Conditions, medicines and genes

Notes

From SNPedia

Notes

rs2305767 (P = 1.16 x 10(-4); OR 1.41, 95% CI 1.18-1.67). We demonstrate significant association of allelic variants in MYO9B with schizophrenia Crohn's disease rs2305767 associated with inflammatory bowel disease (IBD) overall (corrected P-value 0.002, odds ratio [OR] 0.76, 95% confidence interval [CI] 0.67-0.86) However, a 2016 meta-analysis including 8 studies (totaling 2272 cases and 5419 controls) found no significant association for this SNP and celiac disease in Caucasian populations.

Source and license

Adapted from rs2305767 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.