RS111033187 MYO7A
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What This Variant Does
"CLNSIG=4
Associated Conditions
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 2
Rare genetic deafness
Hearing loss
autosomal recessive
Usher syndrome
MYO7A-related disorder
Retinal dystrophy
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 2
Rare genetic deafness
Hearing loss
autosomal recessive
Usher syndrome
MYO7A-related disorder
Other Variants in MYO7A