rs9289231

A SNP in the KALRN gene on chromosome 3. Its most notable genotype is T;T.

Gene
KALRN
Location
Chr 3124,055,231 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
12%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. T;TMost notableNot ratedNo summary available.Typical · 0.075% of people

On SNPedia: (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.

  • AverageT;T 75%
  • European ancestry (Utah)T;T 85%
  • Han Chinese (Beijing)T;T 99%
  • Japanese (Tokyo)T;T 99%
  • Yoruba (Nigeria)T;T 46%
  • African ancestry (Southwest US)T;T 67%
  • Chinese (Denver)T;T 99%
  • Gujarati IndianT;T 84%
  • Luhya (Kenya)T;T 41%
  • Mexican ancestry (Los Angeles)T;T 83%
  • Maasai (Kenya)T;T 48%
  • TuscanT;T 78%

Other KALRN SNPs

All KALRN SNPs

Notes

From SNPedia

Notes

In a study of early onset coronary artery disease, rs9289231, the risk allele of this SNP, located in the kalirin KALRN gene, was associated with increased odds (OR 2.1), and also for increased atherosclerosis burden.

Source and license

Adapted from rs9289231 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.