Gene: PLPP3 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17114036
rs17114036
PLPP3
0.800 GeneticVariation GWASCAT Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. 24262325

2014
dbSNP: rs17114036
rs17114036
PLPP3
A 0.800 GeneticVariation GWASCAT Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. 21378990

2011
dbSNP: rs17114036
rs17114036
PLPP3
A 0.800 GeneticVariation GWASDB Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. 21378990

2011
dbSNP: rs17114046
rs17114046
PLPP3
0.800 GeneticVariation GWASDB A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. 21378988

2011
dbSNP: rs17114046
rs17114046
PLPP3
0.800 GeneticVariation GWASCAT A genome-wide association study in europeans and South asians identifies 5 new Loci for coronary artery disease. 21846871

2011
dbSNP: rs17114046
rs17114046
PLPP3
0.800 GeneticVariation GWASDB A genome-wide association study in europeans and South asians identifies 5 new Loci for coronary artery disease. 21846871

2011
dbSNP: rs17114046
rs17114046
PLPP3
0.800 GeneticVariation GWASCAT A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. 21378988

2011
dbSNP: rs2404715
rs2404715
PLPP3
0.700 GeneticVariation GWASDB Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. 21378990

2011
dbSNP: rs72664392
rs72664392
PLPP3
0.010 GeneticVariation BEFREE A further gender-based subgroup analysis revealed significant associations of APOE rs7259620 and PPAP2B rs72664392 with CHD in males (genotype: χ2=8.379, df=2, p=0.015; allele: χ2=5.190, df=1, p=0.023; recessive model: χ2=19.3, df=1, p<0.0001) and females (genotype: χ2=9.878, df=2, p=0.007), respectively. 29848931

2018
dbSNP: rs12566304
rs12566304
PLPP3
0.010 GeneticVariation BEFREE In the female subgroup, rs12566304 was associated with a decreased CHD risk in the codominant model (p = 0.038) and overdominant model (p = 0.031). 28061459

2017
dbSNP: rs1759752
rs1759752
PLPP3
0.010 GeneticVariation BEFREE Additionally, the "GC" haplotypes of rs1759752 and rs1930760 were protective against CHD in males. 28061459

2017
dbSNP: rs1930760
rs1930760
PLPP3
0.010 GeneticVariation BEFREE Additionally, the "GC" haplotypes of rs1759752 and rs1930760 were protective against CHD in males. 28061459

2017