RS397518048 USH2A

Health Risk Chr 1:215817143
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Usher syndrome
Inborn genetic diseases
Usher syndrome type 2
Retinal dystrophy
Usher syndrome type 2A
Retinitis pigmentosa
Retinitis pigmentosa 39
USH2A-related disorder
Rare genetic deafness
Usher syndrome
Inborn genetic diseases
Usher syndrome type 2
Retinal dystrophy
Usher syndrome type 2A
Other Variants in USH2A
rs80338903 rs397518008 rs111033367 rs121912598 rs121912599 rs80338902 rs111033364 rs111033272 rs121912600 rs587776538
Ask Dr. Hemsworth about this variant