RS104893768 RHO

Health Risk Chr 3:129528801
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What This Variant Does
"[OMIM:?]
Associated Conditions
Retinitis pigmentosa 4
Pigmentary retinal dystrophy
Congenital stationary night blindness autosomal dominant 1
Retinal dystrophy
RHO-related disorder
Retinal dystrophy
Retinitis pigmentosa 4
Pigmentary retinal dystrophy
Congenital stationary night blindness autosomal dominant 1
Retinal dystrophy
RHO-related disorder
Retinal dystrophy
Other Variants in RHO
rs29001566 rs29001637 rs28933394 rs104893769 rs104893771 rs104893772 rs104893773 rs104893779 rs104893774 rs104893776
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