RS369522997 USH2A
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What This Variant Does
"CLNSIG=4
Associated Conditions
Usher syndrome type 2A
Retinitis pigmentosa 39
Usher syndrome
Rare genetic deafness
Retinal dystrophy
Retinitis pigmentosa
Usher syndrome type 2A
Retinitis pigmentosa 39
Usher syndrome
Rare genetic deafness
Retinal dystrophy
Retinitis pigmentosa
Other Variants in USH2A