RS111033174 MYO7A
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What This Variant Does
"Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 2
Usher syndrome type 1B
Retinal dystrophy
MYO7A-related disorder
Autosomal dominant nonsyndromic hearing loss 11
Usher syndrome type 1
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 2
Usher syndrome type 1B
Retinal dystrophy
MYO7A-related disorder
Autosomal dominant nonsyndromic hearing loss 11
Usher syndrome type 1
Other Variants in MYO7A