RS2276278 MYO7A

Health Risk Chr 11:77161122 snv splice region variant
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Associated Conditions
Autosomal dominant nonsyndromic hearing loss 11
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 2
MYO7A-related disorder
Autosomal dominant nonsyndromic hearing loss 11
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 2
MYO7A-related disorder
Population Frequencies
gnomAD ALL
92.8%
1kG AFR
81.3%
1kG ALL
84.6%
1kG AMR
86.9%
1kG EAS
28.2%
1kG EUR
94.4%
1kG SAS
90.7%
Other Variants in MYO7A
rs121965079 rs41298133 rs1555062984 rs28934610 rs121965080 rs121965081 rs2135550200 rs121965082 rs2135478294 rs121965083
Ask Dr. Hemsworth about this variant