Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1333047
rs1333047
CDKN2B-AS1
0.010 GeneticVariation BEFREE The 9p21.3 SNP rs1333047 SNP was associated with increased ASCVD in FH subjects. 28502497

2018
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.010 GeneticVariation BEFREE In aDNA extracted from the same Korean mummy, we identified the risk alleles of seven different SNPs (rs5351, rs10757274, rs2383206, rs2383207, rs10757278, rs4380028 and rs1333049) that had already been revealed to be the major risk loci of ASCVD in East Asian populations. 28813480

2017
dbSNP: rs1333049
rs1333049
CDKN2B-AS1
0.010 GeneticVariation BEFREE In aDNA extracted from the same Korean mummy, we identified the risk alleles of seven different SNPs (rs5351, rs10757274, rs2383206, rs2383207, rs10757278, rs4380028 and rs1333049) that had already been revealed to be the major risk loci of ASCVD in East Asian populations. 28813480

2017
dbSNP: rs4380028
rs4380028
MORF4L1
0.010 GeneticVariation BEFREE In aDNA extracted from the same Korean mummy, we identified the risk alleles of seven different SNPs (rs5351, rs10757274, rs2383206, rs2383207, rs10757278, rs4380028 and rs1333049) that had already been revealed to be the major risk loci of ASCVD in East Asian populations. 28813480

2017
dbSNP: rs4731702
rs4731702
LOC105375508
0.010 GeneticVariation BEFREE The rs4731702-T allele was also associated with a decreased risk of ASCVD with an OR of 0.78 (Pmeta-analysis<5.43×10(-4)). 22702842

2012