RS397515359 USH1C
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What This Variant Does
"CLNSIG=5
Associated Conditions
Usher syndrome type 1C
Usher syndrome type 1
Usher syndrome
Retinitis pigmentosa
Retinal dystrophy
Autosomal recessive nonsyndromic hearing loss 18A
Hearing loss
autosomal recessive
Rare genetic deafness
USH1C-related disorder
Autosomal recessive nonsyndromic hearing loss 18A
Usher syndrome type 1C
Usher syndrome type 1
Usher syndrome
Retinitis pigmentosa
Other Variants in USH1C