Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
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0.830 | GeneticVariation | BEFREE | In UK non CHD, UK CHD, Pakistani non CHD and Pakistani CHD respectively, for rs646776, per risk allele increase in LDL-C(mmol/l) was 0.18(0.04), 0.06(0.11), 0.15(0.04) and 0.27(0.06) respectively. | 27112212 | 2016 |
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0.830 | GeneticVariation | BEFREE | No significant associations were observed between the other two SNPs in loci 1p13 (rs599839 and rs646776) and CHD mortality in either gender. | 24728607 | 2014 |
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0.830 | GeneticVariation | BEFREE | Five single-nucleotide polymorphisms, rs4977574 (CDKN2A/2B), rs12526453 (PHACTR1), rs646776 (CELSR2-PSRC1-SORT1), rs2259816 (HNF1A), and rs11206510 (PCSK9) showed directionally consistent associations with CHD in the 3 studies, with combined odds ratios (ORs) ranging from 1.17 to 1.25 (p = 0.03 to 0.0002). | 22152955 | 2011 |
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T | 0.830 | GeneticVariation | GWASCAT | Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. | 21239051 | 2011 |
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T | 0.830 | GeneticVariation | GWASCAT | A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. | 21378988 | 2011 |
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T | 0.830 | GeneticVariation | GWASDB | A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. | 21378988 | 2011 |
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0.830 | GeneticVariation | GWASDB | Large-scale gene-centric analysis identifies novel variants for coronary artery disease. | 21966275 | 2011 |
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0.830 | GeneticVariation | GWASDB | Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. | 21347282 | 2011 |