Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2259816
rs2259816
HNF1A
0.820 GeneticVariation GWASDB Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. 21347282

2011
dbSNP: rs2259816
rs2259816
HNF1A
0.820 GeneticVariation BEFREE Five single-nucleotide polymorphisms, rs4977574 (CDKN2A/2B), rs12526453 (PHACTR1), rs646776 (CELSR2-PSRC1-SORT1), rs2259816 (HNF1A), and rs11206510 (PCSK9) showed directionally consistent associations with CHD in the 3 studies, with combined odds ratios (ORs) ranging from 1.17 to 1.25 (p = 0.03 to 0.0002). 22152955

2011
dbSNP: rs2259816
rs2259816
HNF1A
0.820 GeneticVariation BEFREE In the LURIC Study cohort the A-allele of rs2259816 is associated with decreased CRP but not with coronary artery disease. 21062467

2010
dbSNP: rs2259816
rs2259816
HNF1A
T 0.820 GeneticVariation GWASCAT New susceptibility locus for coronary artery disease on chromosome 3q22.3. 19198612

2009
dbSNP: rs2259816
rs2259816
HNF1A
T 0.820 GeneticVariation GWASDB New susceptibility locus for coronary artery disease on chromosome 3q22.3. 19198612

2009