Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2383207
rs2383207
CDKN2B-AS1
0.040 GeneticVariation BEFREE The association of polymorphic variants, rs2267788, rs1333049 and rs2383207 with coronary artery disease, its severity and presentation in North Indian population. 29309886

2018
dbSNP: rs2383207
rs2383207
CDKN2B-AS1
0.040 GeneticVariation BEFREE Some studies investigated the association of antisense non-coding RNA in the INK4 locus (ANRIL) rs2383207 polymorphism with coronary artery disease (CAD) risk. 27894414

2016
dbSNP: rs2383207
rs2383207
CDKN2B-AS1
0.040 GeneticVariation BEFREE Conclusions The rs10757278 and rs2383207 variants are determinants for early-onset coronary artery disease. 18459066

2009
dbSNP: rs2383207
rs2383207
CDKN2B-AS1
0.040 GeneticVariation BEFREE The SNP rs2383207 on chromosome 9p21 is significantly associated with CHD in Chinese. 18757290

2008