RS397516326 MYO7A

Health Risk Chr 11:77208776
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What This Variant Does
"CLNSIG=5
Associated Conditions
Usher syndrome type 1
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 2
Retinal dystrophy
Usher syndrome type 1B
Autosomal dominant nonsyndromic hearing loss 11
See cases
Usher syndrome type 1
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 2
Retinal dystrophy
Usher syndrome type 1B
Autosomal dominant nonsyndromic hearing loss 11
See cases
Other Variants in MYO7A
rs121965079 rs41298133 rs1555062984 rs28934610 rs121965080 rs121965081 rs2135550200 rs121965082 rs2135478294 rs121965083
Ask Dr. Hemsworth about this variant