Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7412
rs7412
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.730 GeneticVariation BEFREE Aim was to estimate the genotypic distribution and risk allele frequencies of 13 Coronary Artery Disease (CAD) risk Single Nucleotide Polymorphisms in loci identified by the CARDIoGRAMplusC4D consortium namely MIA3 rs17465637; 9p21 rs10757274; CXCL12 rs1746048; APOA5 rs662799; APOB rs1042031; LPA rs3798220; LPA 10455872; MRAS rs9818870; LPL rs328; SORT1 rs646776; PCSK9 rs11591147; APOE rs429358; APOE rs7412 in Pakistani PCAD patients and controls. 28705542

2019

dbSNP: rs7412
rs7412
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
T 0.730 GeneticVariation GWASCAT Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies. 30104761

2018

dbSNP: rs7412
rs7412
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
T 0.730 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778

2018

dbSNP: rs7412
rs7412
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.730 GeneticVariation BEFREE The univariate analysis indicated that the five variants; rs1800595 (FVR2; factor 5), rs1801133 (MTHFR; 5,10-methylenetetrahydrofolate reductase), rs5918 (HPA-1; human platelet antigen 1), rs1799752 (ACE; angiotensin-converting enzyme), and rs7412 and rs429358 (ApoE; apolipoprotein E) were significantly associated with CAD susceptibility under different genetic models. 28086795

2017

dbSNP: rs7412
rs7412
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
C 0.730 GeneticVariation GWASCAT Association analyses based on false discovery rate implicate new loci for coronary artery disease. 28714975

2017

dbSNP: rs7412
rs7412
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.730 GeneticVariation BEFREE CAD association was replicated and/or verified for 4 loci: SORT1 rs611917 (p=1.7 × 10(-8)), APOA5 rs662799 (p=0.0014), LDLR rs1433099 (p=2.1 × 10(-7)), and APOE rs7412 (p=6.1 × 10(-13)). 23050023

2012