RS111033367 USH2A

Health Risk Chr 1:216190280
Upload your DNA to see your genotype for this variant.
What This Variant Does
"aka c.4338_4339delCT (p.Cys1447Glnfs) This mutation in the USH2A gene is the major cause of Usher sy...
Associated Conditions
Usher syndrome type 2A
USH2A-related disorder
Usher syndrome
Retinal dystrophy
Retinitis pigmentosa 39
Usher syndrome type 2A
USH2A-related disorder
Usher syndrome
Retinal dystrophy
Retinitis pigmentosa 39
Other Variants in USH2A
rs80338903 rs397518008 rs121912598 rs121912599 rs80338902 rs111033364 rs111033272 rs121912600 rs587776538 rs111033334
Ask Dr. Hemsworth about this variant