RS121965079 MYO7A

Health Risk Chr 11:77156068 snv stop gained
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What This Variant Does
"[OMIM:?]
Associated Conditions
Usher syndrome type 1B
Usher syndrome
Autosomal recessive nonsyndromic hearing loss 2
Autosomal recessive nonsyndromic hearing loss 2
Usher syndrome type 1
Autosomal dominant nonsyndromic hearing loss 11
Usher syndrome type 1B
Retinal dystrophy
Usher syndrome type 1B
Usher syndrome
Autosomal recessive nonsyndromic hearing loss 2
Autosomal recessive nonsyndromic hearing loss 2
Usher syndrome type 1
Autosomal dominant nonsyndromic hearing loss 11
Usher syndrome type 1B
Population Frequencies
gnomAD ALL
100%
1kG AFR
100%
1kG ALL
0%
1kG AMR
100%
1kG EAS
100%
1kG EUR
0.1%
1kG SAS
100%
Other Variants in MYO7A
rs41298133 rs1555062984 rs28934610 rs121965080 rs121965081 rs2135550200 rs121965082 rs2135478294 rs121965083 rs35689081
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