RS80338828 MYH9
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What This Variant Does
"A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosac...
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 17
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
Autosomal dominant nonsyndromic hearing loss 17
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
Other Variants in MYH9