RS111033417 USH2A

Health Risk Chr 1:215674597 snv stop gained
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What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Retinal dystrophy
Retinitis pigmentosa 39
Rare genetic deafness
Retinal dystrophy
Retinitis pigmentosa 39
Population Frequencies
gnomAD ALL
100%
Other Variants in USH2A
rs80338903 rs397518008 rs111033367 rs121912598 rs121912599 rs80338902 rs111033364 rs111033272 rs121912600 rs587776538
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