RS782165016 MYO7A

Health Risk Chr 11:77179738
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Associated Conditions
Usher syndrome type 1B
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 11
Nonsyndromic genetic hearing loss
Usher syndrome type 1B
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 11
Nonsyndromic genetic hearing loss
Other Variants in MYO7A
rs121965079 rs41298133 rs1555062984 rs28934610 rs121965080 rs121965081 rs2135550200 rs121965082 rs2135478294 rs121965083
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