RS111033178 MYO7A
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What This Variant Does
"Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of geneti...
Associated Conditions
Usher syndrome type 1
Usher syndrome
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 2
Autosomal dominant nonsyndromic hearing loss 11
Retinal dystrophy
Usher syndrome type 1B
MYO7A-related disorder
Usher syndrome type 1
Usher syndrome
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 2
Autosomal dominant nonsyndromic hearing loss 11
Retinal dystrophy
Usher syndrome type 1B
Population Frequencies
gnomAD ALL
100%
Other Variants in MYO7A