RS780308389 USH2A

Health Risk Chr 1:216325393
Upload your DNA to see your genotype for this variant.
Associated Conditions
Usher syndrome
Retinal dystrophy
Retinitis pigmentosa 39
Usher syndrome type 2A
USH2A-related disorder
Rare genetic deafness
Monogenic hearing loss
Usher syndrome
Retinal dystrophy
Retinitis pigmentosa 39
Usher syndrome type 2A
USH2A-related disorder
Rare genetic deafness
Monogenic hearing loss
Other Variants in USH2A
rs80338903 rs397518008 rs111033367 rs121912598 rs121912599 rs80338902 rs111033364 rs111033272 rs121912600 rs587776538
Ask Dr. Hemsworth about this variant