RS376040199 MYH9
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 17
MYH9-related disorder
Ovarian serous cystadenocarcinoma
Autosomal dominant nonsyndromic hearing loss 17
MYH9-related disorder
Ovarian serous cystadenocarcinoma
Other Variants in MYH9