RS28934610 MYO7A

Health Risk Chr 11:77156904
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What This Variant Does
"[OMIM:USHER SYNDROME, TYPE IB]
Associated Conditions
Usher syndrome type 1B
Rare genetic deafness
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 2
Retinal dystrophy
Usher syndrome
Usher syndrome type 1B
Rare genetic deafness
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 2
Retinal dystrophy
Usher syndrome
Other Variants in MYO7A
rs121965079 rs41298133 rs1555062984 rs121965080 rs121965081 rs2135550200 rs121965082 rs2135478294 rs121965083 rs35689081
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