Variant: rs2259816 

    present in Gene: HNF1A
    present in Chromosome: 12
    Position on Chromosome: 120997784
    Alleles of this Variant: G/A;T

rs2259816 in HNF1A gene and C-reactive protein measurement PMID 31217584 2019 Genetic analyses of diverse populations improves discovery for complex traits.

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?

PMID 22939635 2012 Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women.

PMID 24763700 2014 New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis.

rs2259816 in HNF1A gene and Coronary heart disease PMID 19198612 2009 New susceptibility locus for coronary artery disease on chromosome 3q22.3.

PMID 21347282 2011 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

rs2259816 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.