RS62638193 RDH5

Health Risk Chr 12:55724427
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What This Variant Does
"[OMIM:?]
Associated Conditions
Fundus albipunctatus
autosomal recessive
Pigmentary retinal dystrophy
Congenital stationary night blindness
Fundus albipunctatus
autosomal recessive
Pigmentary retinal dystrophy
Congenital stationary night blindness
Other Variants in RDH5
rs62638191 rs111033593 rs104894373 rs62638194 rs267607006 rs104894374 rs774122562 rs781112960 rs62638195 rs769035379
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