RS774122562 RDH5

Health Risk Chr 12:55721469
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What This Variant Does
"CLNSIG=5
Associated Conditions
Pigmentary retinal dystrophy
Fundus albipunctatus
autosomal recessive
Pigmentary retinal dystrophy
Fundus albipunctatus
autosomal recessive
Other Variants in RDH5
rs62638191 rs62638193 rs111033593 rs104894373 rs62638194 rs267607006 rs104894374 rs781112960 rs62638195 rs769035379
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