Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1260326
rs1260326
GCKR
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.820 GeneticVariation GWASDB Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci. 23505323

2013
dbSNP: rs1260326
rs1260326
GCKR
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		T 0.820 GeneticVariation GWASDB Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. 20657596

2010
dbSNP: rs1260326
rs1260326
GCKR
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		T 0.820 GeneticVariation GWASCAT Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. 20657596

2010