RS104893793 RHO

Health Risk Chr 3:129531005
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What This Variant Does
"[OMIM:?]
Associated Conditions
Retinitis pigmentosa 4
Retinal dystrophy
Congenital stationary night blindness autosomal dominant 1
Cone-rod dystrophy
Retinitis pigmentosa
Retinitis pigmentosa 4
Retinal dystrophy
Retinitis pigmentosa 4
Retinal dystrophy
Congenital stationary night blindness autosomal dominant 1
Cone-rod dystrophy
Retinitis pigmentosa
Retinitis pigmentosa 4
Retinal dystrophy
Other Variants in RHO
rs104893768 rs29001566 rs29001637 rs28933394 rs104893769 rs104893771 rs104893772 rs104893773 rs104893779 rs104893774
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