RS121965080 MYO7A
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Usher syndrome type 1B
Usher syndrome type 1
Autosomal dominant nonsyndromic hearing loss 11
Autosomal recessive nonsyndromic hearing loss 2
Usher syndrome type 1B
Usher syndrome type 1
Autosomal dominant nonsyndromic hearing loss 11
Autosomal recessive nonsyndromic hearing loss 2
Other Variants in MYO7A