Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1049673
rs1049673
CD36
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance 		0.010 GeneticVariation BEFREE The major findings of this study were that rs1049673 was found associated with IFG/IGT and T2D in essential hypertension patients (Pco = 0.028; Pdom = 0.015). 22869067

2012