RDH8, retinol dehydrogenase 8, 50700

N. diseases: 6; N. variants: 3
Disease: Severe myopia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2233789
rs2233789
Entrez Id: 50700
Gene Symbol: RDH8
RDH8
CUI: C0271183
Disease:
Severe myopia 		0.010 GeneticVariation BEFREE SNPs RDH851 (rs2233789) and RDH8E5a (rs1644731) both did not show association with high myopia. 21043051 2010