RS117966637 MYO7A

Health Risk Chr 11:77189441 snv missense variant
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Associated Conditions
Autosomal recessive nonsyndromic hearing loss 2
Usher syndrome type 1
Autosomal dominant nonsyndromic hearing loss 11
MYO7A-related disorder
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 2
Usher syndrome type 1
Autosomal dominant nonsyndromic hearing loss 11
MYO7A-related disorder
Usher syndrome type 1
Population Frequencies
gnomAD ALL
100%
1kG AFR
100%
1kG ALL
0.1%
1kG AMR
100%
1kG EAS
0.4%
1kG EUR
100%
1kG SAS
100%
Other Variants in MYO7A
rs121965079 rs41298133 rs1555062984 rs28934610 rs121965080 rs121965081 rs2135550200 rs121965082 rs2135478294 rs121965083
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