RS1302814429 MYH9

Health Risk Chr 22:36285173
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 17
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 17
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
Other Variants in MYH9
rs80338835 rs80338834 rs80338829 rs121913655 rs80338831 rs121913656 rs80338826 rs80338828 rs587776808 rs80338827
Ask Dr. Hemsworth about this variant