RS104893790 RHO

Health Risk Chr 3:129529002
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital stationary night blindness autosomal dominant 1
Pigmentary retinal dystrophy
Retinal dystrophy
Congenital stationary night blindness autosomal dominant 1
Pigmentary retinal dystrophy
Retinal dystrophy
Other Variants in RHO
rs104893768 rs29001566 rs29001637 rs28933394 rs104893769 rs104893771 rs104893772 rs104893773 rs104893779 rs104893774
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