Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1122608
rs1122608
0.720 GeneticVariation BEFREE The rs1122608 is associated with the risk of CAD and TG level. 27664493

2016

dbSNP: rs1122608
rs1122608
0.720 GeneticVariation BEFREE A single nucleotide polymorphism (SNP) rs1122608 on chromosome 19p13.2 and in the BRG1/SMARCA4 gene was previously associated with coronary artery disease (CAD). 24190014

2014

dbSNP: rs1122608
rs1122608
T 0.720 GeneticVariation GWASDB Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. 24262325

2014