RS111033232 MYO7A

Health Risk Chr 11:77208452 delins inframe deletion
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Usher syndrome type 1
Usher syndrome type 1B
Autosomal recessive nonsyndromic hearing loss 2
Retinitis pigmentosa
Rare genetic deafness
Usher syndrome type 1
Usher syndrome type 1B
Autosomal recessive nonsyndromic hearing loss 2
Retinitis pigmentosa
Population Frequencies
gnomAD ALL
100%
Other Variants in MYO7A
rs121965079 rs41298133 rs1555062984 rs28934610 rs121965080 rs121965081 rs2135550200 rs121965082 rs2135478294 rs121965083
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