Variant: rs1183910 

    present in Gene: HNF1A
    present in Chromosome: 12
    Position on Chromosome: 120983004
    Alleles of this Variant: G/A

rs1183910 in HNF1A gene and C-reactive protein measurement PMID 31217584 2019 Genetic analyses of diverse populations improves discovery for complex traits.

PMID 19567438 2009 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease.

PMID 21647738 2012 Genome-wide association with C-reactive protein levels in CLHNS: evidence for the CRP and HNF1A loci and their interaction with exposure to a pathogenic environment.

PMID 27286809 2016 Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation.

PMID 21300955 2011 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.

PMID 23844046 2013 Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore?

rs1183910 in HNF1A gene and Low density lipoprotein cholesterol measurement PMID 27286809 2016 Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation.

rs1183910 in HNF1A gene and Pseudocholinesterase Measurement PMID 21943158 2011 Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.

rs1183910 in HNF1A gene and Serum total cholesterol measurement PMID 27286809 2016 Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation.