RS117390537 MYH2

Health Risk Chr 17:10533542 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Population Frequencies
gnomAD ALL
0.1%
1kG AFR
100%
1kG ALL
99.9%
1kG AMR
0.3%
1kG EAS
100%
1kG EUR
0.3%
1kG SAS
0.1%
Other Variants in MYH2
Ask Dr. Hemsworth about this variant