RS1064797153 USH1C

Health Risk Chr 11:17523239
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What This Variant Does
"CLNSIG=4
Associated Conditions
Usher syndrome type 1C
Autosomal recessive nonsyndromic hearing loss 18A
Usher syndrome type 2
Usher syndrome type 1C
Autosomal recessive nonsyndromic hearing loss 18A
Usher syndrome type 2
Other Variants in USH1C
rs1480243085 rs397515359 rs55983148 rs151045328 rs1403777293 rs121908370 rs1592002789 rs41282932 rs397514500 rs778110397
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