RS782077721 MYO7A

Health Risk Chr 11:77162915
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Associated Conditions
Inborn genetic diseases
Usher syndrome type 1
Retinal dystrophy
Usher syndrome type 1B
Autosomal dominant nonsyndromic hearing loss 11
Autosomal recessive nonsyndromic hearing loss 2
Inborn genetic diseases
Usher syndrome type 1
Retinal dystrophy
Usher syndrome type 1B
Autosomal dominant nonsyndromic hearing loss 11
Autosomal recessive nonsyndromic hearing loss 2
Other Variants in MYO7A
rs121965079 rs41298133 rs1555062984 rs28934610 rs121965080 rs121965081 rs2135550200 rs121965082 rs2135478294 rs121965083
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