RS111033259 MYO7A

Health Risk Chr 11:77198596 delins protein altering variant
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What This Variant Does
"CLNSIG=255
Associated Conditions
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 11
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 2
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 11
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 2
Other Variants in MYO7A
rs121965079 rs41298133 rs1555062984 rs28934610 rs121965080 rs121965081 rs2135550200 rs121965082 rs2135478294 rs121965083
Ask Dr. Hemsworth about this variant