RS748117872 MYH9
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 17
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
MYH9-related disorder
Autosomal dominant nonsyndromic hearing loss 17
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
MYH9-related disorder
Other Variants in MYH9