RS139134727 MYH9

Health Risk Chr 22:36289245 snv missense variant
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Associated Conditions
MYH9-related disorder
Autosomal dominant nonsyndromic hearing loss 17
MYH9-related disorder
Autosomal dominant nonsyndromic hearing loss 17
Population Frequencies
gnomAD ALL
0.3%
1kG AFR
100%
1kG ALL
0%
1kG AMR
100%
1kG EAS
100%
1kG EUR
0.1%
1kG SAS
99.9%
Other Variants in MYH9
rs80338835 rs80338834 rs80338829 rs121913655 rs80338831 rs121913656 rs80338826 rs80338828 rs587776808 rs80338827
Ask Dr. Hemsworth about this variant