RS199897298 MYO7A
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 2
Retinal dystrophy
Hearing loss
Usher syndrome type 1B
Autosomal dominant nonsyndromic hearing loss 11
Usher syndrome type 1
Hereditary breast ovarian cancer syndrome
MYO7A-related disorder
Monogenic hearing loss
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 2
Retinal dystrophy
Hearing loss
Usher syndrome type 1B
Other Variants in MYO7A