RS797044512 MYO7A
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 11
Bilateral sensorineural hearing impairment
MYO7A-related disorder
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 11
Bilateral sensorineural hearing impairment
MYO7A-related disorder
Other Variants in MYO7A