RS771279169 USH1C

Health Risk Chr 11:17522927
Upload your DNA to see your genotype for this variant.
Associated Conditions
Usher syndrome type 1C
Autosomal recessive nonsyndromic hearing loss 18A
Usher syndrome type 1C
Autosomal recessive nonsyndromic hearing loss 18A
Other Variants in USH1C
rs1480243085 rs397515359 rs55983148 rs151045328 rs1403777293 rs121908370 rs1592002789 rs41282932 rs397514500 rs778110397
Ask Dr. Hemsworth about this variant