Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2107595
rs2107595
0.020 GeneticVariation BEFREE Previous results suggest a role of altered <i>HDAC9</i> expression levels as the underlying disease mechanism. rs2107595, the lead single nucleotide polymorphism for stroke and coronary artery disease resides in noncoding DNA and colocalizes with histone modification marks suggestive of enhancer elements. 31500558

2019

dbSNP: rs2107595
rs2107595
0.020 GeneticVariation BEFREE Subgroup and multifactor dimensionality reduction analyses (MDR) further found the gene-environment interactions among SNP rs2107595, body mass index, type 2 diabetes and hyperlipidemia in CAD risk and the severity of coronary atherosclerosis. 27494404

2016