RS111033364 USH2A
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What This Variant Does
"[OMIM:?]
Associated Conditions
Usher syndrome type 2A
Hearing impairment
Retinitis pigmentosa 39
Congenital sensorineural hearing impairment
Retinitis pigmentosa
Retinal dystrophy
Rare genetic deafness
Usher syndrome
Usher syndrome type 2
USH2A-related disorder
Usher syndrome type 3A
See cases
Retinal disorder
Usher syndrome type 2A
Hearing impairment
Other Variants in USH2A