RS138138689 USH1C

Health Risk Chr 11:17527222
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What This Variant Does
"CLNSIG=5
Associated Conditions
Usher syndrome type 1C
Autosomal recessive nonsyndromic hearing loss 18A
Inborn genetic diseases
Usher syndrome type 1C
Autosomal recessive nonsyndromic hearing loss 18A
Usher syndrome type 1
USH1C-related disorder
Usher syndrome type 1C
Autosomal recessive nonsyndromic hearing loss 18A
Inborn genetic diseases
Usher syndrome type 1C
Autosomal recessive nonsyndromic hearing loss 18A
Usher syndrome type 1
USH1C-related disorder
Other Variants in USH1C
rs1480243085 rs397515359 rs55983148 rs151045328 rs1403777293 rs121908370 rs1592002789 rs41282932 rs397514500 rs778110397
Ask Dr. Hemsworth about this variant