RS111033272 USH2A

Health Risk Chr 1:216325499
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What This Variant Does
"CLNSIG=5
Associated Conditions
Usher syndrome type 2A
Abnormal macular morphology
Pigmentary retinopathy
Retinal pigment epithelial atrophy
Blindness
Rod-cone dystrophy
Retinitis pigmentosa 39
Rare genetic deafness
Retinal dystrophy
Usher syndrome type 2
Usher syndrome type 2A
Abnormal macular morphology
Pigmentary retinopathy
Retinal pigment epithelial atrophy
Blindness
Other Variants in USH2A
rs80338903 rs397518008 rs111033367 rs121912598 rs121912599 rs80338902 rs111033364 rs121912600 rs587776538 rs111033334
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