RS62638191 RDH5

Health Risk Chr 12:55724028
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What This Variant Does
"[OMIM:?]
Associated Conditions
Fundus albipunctatus
autosomal recessive
Pigmentary retinal dystrophy
See cases
Congenital stationary night blindness
RDH5-related disorder
Retinal dystrophy
Retinitis punctata albescens
Fundus albipunctatus
autosomal recessive
Pigmentary retinal dystrophy
See cases
Congenital stationary night blindness
RDH5-related disorder
Retinal dystrophy
Other Variants in RDH5
rs62638193 rs111033593 rs104894373 rs62638194 rs267607006 rs104894374 rs774122562 rs781112960 rs62638195 rs769035379
Ask Dr. Hemsworth about this variant