RS397515411 CIB2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 48
Hearing loss
autosomal recessive
Usher syndrome type 1J
Autosomal recessive nonsyndromic hearing loss 48
Hearing loss
autosomal recessive
Usher syndrome type 1J
Other Variants in CIB2