rs2032487

A SNP in the MYH9 gene on chromosome 22. Its most notable genotype is T;T: common in complete genomics

Gene
MYH9
Location
Chr 2236,299,382 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
18%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in complete genomicsTypical · 0.068% 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 3 HapMap populations.

  • AverageT;T 68%
  • Han Chinese (Beijing)T;T 100%
  • Japanese (Tokyo)T;T 100%
  • Yoruba (Nigeria)T;T 5%

Other MYH9 SNPs

All MYH9 SNPs

Source and license

Adapted from rs2032487 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.