Geno
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Mag
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Summary
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(C;C)
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0
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common in complete genomics
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per the 23andMe blog, the minor allele of this SNP (T) was associated with decreased HDL cholesterol
GWAS snp
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PMID
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[PMID 19060906]
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Trait
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HDL cholesterol
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Title
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Common variants at 30 loci contribute to polygenic dyslipidemia
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Risk Allele
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T
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P-val
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8E-10
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Odds Ratio
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0.19 [0.09-0.29] SD decrease
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[PMID 19748811] Influence of hepatocyte nuclear factor 4alpha (HNF4alpha) gene variants on the risk of type 2 diabetes: A meta-analysis in 49,577 individuals
GWAS snp
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PMID
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[PMID 21300955]
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Trait
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Title
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Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels
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Risk Allele
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C
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P-val
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2E-9
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Odds Ratio
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0.0880 [0.06-0.12] unit increase
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GWAS snp
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PMID
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[PMID 20686565]
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Trait
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Title
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Biological, clinical and population relevance of 95 loci for blood lipids.
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Risk Allele
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T
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P-val
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1E-15
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Odds Ratio
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1.8800 None
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[PMID 16186411] Variants in hepatocyte nuclear factor 4alpha are modestly associated with type 2 diabetes in Pima Indians.
[PMID 18660489] Multiple genetic variants along candidate pathways influence plasma high-density lipoprotein cholesterol concentrations.
[PMID 19915572] Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.
[PMID 19951432] Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease.
[PMID 20385826] Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).
GWAS snp
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PMID
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[PMID 22939635]
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Trait
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C-reactive protein
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Title
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Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women.
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Risk Allele
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T
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P-val
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8E-6
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Odds Ratio
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.27 [0.15-0.39] (unit decrease)
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