LPA, lipoprotein(a), 4018

N. diseases: 340; N. variants: 49
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0010068
Disease:
Coronary heart disease
0.830 GeneticVariation BEFREE In the replication cohort, rs10455872 was also associated with CHD events (odds ratio, 1.71; 95% confidence interval, 1.14-2.57; P=0.009). 29703846 2018
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0010068
Disease:
Coronary heart disease
G 0.830 GeneticVariation GWASCAT Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. 28753643 2017
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0010068
Disease:
Coronary heart disease
0.830 GeneticVariation GWASCAT Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. 24262325 2014
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0010068
Disease:
Coronary heart disease
0.830 GeneticVariation BEFREE Extreme lipoprotein(a) levels or corresponding LPA KIV-2/rs10455872 risk genotypes substantially improved MI and CHD risk prediction. 23375930 2013
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0010068
Disease:
Coronary heart disease
0.830 GeneticVariation BEFREE For the best SNP rs10455872 for plasma Lp(a) levels, the OR for CHD, CVD, and CVD death was 0.94 (95% CI: 0.69-1.28), 0.97 (0.72-1.29), and 1.23 (0.79-1.92), respectively. 21900290 2012
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0010068
Disease:
Coronary heart disease
0.830 GeneticVariation GWASDB Large-scale gene-centric analysis identifies novel variants for coronary artery disease. 21966275 2011
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0428791
Disease:
Aortic valve calcification
0.820 GeneticVariation BEFREE In this population, carriers of rs10455872-G allele had 3.86 and 2.54 higher risk of Lp(a) ≥ 30 mg/dL or presence of AVC, respectively. 31188921 2019
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0428791
Disease:
Aortic valve calcification
G 0.820 GeneticVariation GWASCAT One SNP in the lipoprotein(a) (LPA) locus (rs10455872) reached genomewide significance for the presence of aortic-valve calcification (odds ratio per allele, 2.05; P=9.0×10(-10)), a finding that was replicated in additional white European, African-American, and Hispanic-American cohorts (P<0.05 for all comparisons). 23388002 2013
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0428791
Disease:
Aortic valve calcification
0.820 GeneticVariation GWASDB One SNP in the lipoprotein(a) (LPA) locus (rs10455872) reached genomewide significance for the presence of aortic-valve calcification (odds ratio per allele, 2.05; P=9.0×10(-10)), a finding that was replicated in additional white European, African-American, and Hispanic-American cohorts (P<0.05 for all comparisons). 23388002 2013
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0428791
Disease:
Aortic valve calcification
0.820 GeneticVariation BEFREE One SNP in the lipoprotein(a) (LPA) locus (rs10455872) reached genomewide significance for the presence of aortic-valve calcification (odds ratio per allele, 2.05; P=9.0×10(-10)), a finding that was replicated in additional white European, African-American, and Hispanic-American cohorts (P<0.05 for all comparisons). 23388002 2013
dbSNP: rs3798220
rs3798220
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0010068
Disease:
Coronary heart disease
0.820 GeneticVariation BEFREE Using predefined cutpoints for extreme lipoprotein(a) levels and/or corresponding LPA risk genotypes (kringle IV type 2 [KIV-2]) repeat polymorphism, rs3798220, and rs10455872 single nucleotide polymorphisms), we calculated net reclassification indices from <10% to 10% to 19.9% to ≥20% absolute 10-year MI and CHD risk. 23375930 2013
dbSNP: rs3798220
rs3798220
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0010068
Disease:
Coronary heart disease
0.820 GeneticVariation BEFREE Single nucleotide polymorphisms (SNPs) at the KIF6 (kinesin like protein 6, rs20455 or 719Arg), LPA (lipoprotein(a), rs3798220), TAS2R50 (taste receptor type 2, member 50, rs1376251) and VAMP8 (vesicle-associated membrane protein 8, rs1010) have previously been associated with low density lipoprotein cholesterol (LDL-C) lowering response to statins, coronary heart disease (CHD) at baseline, or CHD events on trial. 22192511 2012
dbSNP: rs3798220
rs3798220
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0010068
Disease:
Coronary heart disease
C 0.820 GeneticVariation GWASCAT Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. 21378990 2011
dbSNP: rs3798220
rs3798220
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0010068
Disease:
Coronary heart disease
0.820 GeneticVariation GWASDB Large-scale gene-centric analysis identifies novel variants for coronary artery disease. 21966275 2011
dbSNP: rs3798220
rs3798220
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0010068
Disease:
Coronary heart disease
C 0.820 GeneticVariation GWASDB Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. 21378990 2011
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement
0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C1445957
Disease:
Serum total cholesterol measurement
0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C1445957
Disease:
Serum total cholesterol measurement
A 0.800 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C1445957
Disease:
Serum total cholesterol measurement
A 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement
A 0.800 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement
A 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement
G 0.800 GeneticVariation GWASCAT Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins. 25350695 2014
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement
0.800 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C1445957
Disease:
Serum total cholesterol measurement
0.800 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs10455872
rs10455872
Entrez Id: 4018
Gene Symbol: LPA
LPA
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement
0.800 GeneticVariation GWASDB Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project. 22629316 2012