RS199968414 MYH9
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Associated Conditions
Autosomal dominant nonsyndromic hearing loss 17
MYH9-related disorder
Inborn genetic diseases
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
Autosomal dominant nonsyndromic hearing loss 17
MYH9-related disorder
Inborn genetic diseases
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
Other Variants in MYH9