rs5750248
A SNP in the MYH9 gene on chromosome 22. Its most notable genotype is C;C: common in complete genomics
- Gene
- MYH9
- Location
- Chr 2236,306,846 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 16%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageC;C 74%
- European ancestry (Utah)C;C 89%
- Han Chinese (Beijing)C;C 100%
- Japanese (Tokyo)C;C 100%
- Yoruba (Nigeria)C;C 5%
Related
Other MYH9 SNPs
- rs2032487T;Tcommon in complete genomicsTypical
- rs2269529T;Tcommon in clinvarTypical
- rs2413396C;Ccommon in clinvarTypical
- rs3752462T;Tcommon in clinvarTypical
- rs4821480T;Tcommon in complete genomicsTypical
- rs4821481T;Tcommon in complete genomicsTypical
- rs5750250A;Acommon in complete genomicsTypical
- rs11912763G;Gcommon in complete genomicsTypical
Source and license
Adapted from rs5750248 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.