RS111033192 MYO7A
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What This Variant Does
"CLNSIG=5
Associated Conditions
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 2
Usher syndrome type 1B
Usher syndrome
MYO7A-related disorder
Autosomal dominant nonsyndromic hearing loss 11
Rare genetic deafness
Usher syndrome type 1
Usher syndrome type 1B
MYO7A-related disorder
Retinal dystrophy
Autosomal dominant nonsyndromic hearing loss 11
Autosomal recessive nonsyndromic hearing loss 2
Monogenic hearing loss
Usher syndrome type 1
Other Variants in MYO7A