Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10455872
rs10455872
LPA
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
LPA
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
LPA
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: rs3798220
rs3798220
LPA
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
LPA
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: rs7767084
rs7767084
LPA
0.710 GeneticVariation BEFREE However, our meta-analysis indicated that rs7767084</span> is not associated with a higher ri</span>sk of CHD. 23653095

2013