RS80338903 USH2A
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What This Variant Does
"CLNSIG=5
Associated Conditions
Usher syndrome type 2A
Retinitis pigmentosa
Retinitis pigmentosa 39
Retinal dystrophy
Usher syndrome
Inborn genetic diseases
Macular dystrophy
USH2A-related disorder
Cone-rod dystrophy
Congenital stationary night blindness
Rare genetic deafness
Monogenic hearing loss
Retinal disorder
Autosomal recessive USH2A-related disorders
Usher syndrome type 2
Other Variants in USH2A