RS80338902 USH2A

Health Risk Chr 1:216247118
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What This Variant Does
"[OMIM:?]
Associated Conditions
Retinitis pigmentosa 39
Retinitis pigmentosa
Usher syndrome type 2A
USH2A-related disorder
Retinal dystrophy
Usher syndrome
Inborn genetic diseases
Autosomal recessive retinitis pigmentosa
Ear malformation
See cases
Retinitis pigmentosa 39
Retinitis pigmentosa
Usher syndrome type 2A
USH2A-related disorder
Retinal dystrophy
Other Variants in USH2A
rs80338903 rs397518008 rs111033367 rs121912598 rs121912599 rs111033364 rs111033272 rs121912600 rs587776538 rs111033334
Ask Dr. Hemsworth about this variant