Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1050106163
rs1050106163
APOE
CUI: C1405854
Disease: Retinitis punctata albescens (disorder)
Retinitis punctata albescens (disorder) 		0.010 GeneticVariation BEFREE Retinitis punctata albescens associated with the Arg135Trp mutation in the rhodopsin gene. 8554077

1996