RS121965079 MYO7A
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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
Other Variants in MYO7A