RS111033233 MYO7A
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 2
Usher syndrome type 1B
Retinal dystrophy
Autosomal dominant nonsyndromic hearing loss 11
Usher syndrome type 1
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 2
Usher syndrome type 1
Autosomal dominant nonsyndromic hearing loss 11
Thyroid cancer
nonmedullary
1
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 2
Other Variants in MYO7A