RS80338835 MYH9
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What This Variant Does
"The gene for May-Hegglin anomaly localizes to a <
Associated Conditions
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
MYH9-related disorder
Abnormal bleeding
Thrombocytopenia
Autosomal dominant nonsyndromic hearing loss 17
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
MYH9-related disorder
Abnormal bleeding
Thrombocytopenia
Autosomal dominant nonsyndromic hearing loss 17
Other Variants in MYH9