RS41282932 USH1C

Health Risk Chr 11:17509546
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 18A
Usher syndrome type 1C
Usher syndrome type 1
Retinal dystrophy
Meniere disease
Optic atrophy
Autosomal recessive nonsyndromic hearing loss 18A
Usher syndrome type 1C
Usher syndrome type 1
Retinal dystrophy
Meniere disease
Optic atrophy
Other Variants in USH1C
rs1480243085 rs397515359 rs55983148 rs151045328 rs1403777293 rs121908370 rs1592002789 rs397514500 rs778110397 rs146333270
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