Variant: rs12777 

    present in Gene: MIR3936HG;SLC22A4
    present in Chromosome: 5
    Position on Chromosome: 132335969
    Alleles of this Variant: C/G

rs12777 in MIR3936HG;SLC22A4 gene and Fibrinogen assay PMID 20031577 2009 Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.

PMID 26561523 2016 A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.

rs12777 in MIR3936HG;SLC22A4 gene and Fibrinogen, CTCAE PMID 20031577 2009 Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.

rs12777 in MIR3936HG;SLC22A4 gene and Glomerular Filtration Rate PMID 31152163 2019 A catalog of genetic loci associated with kidney function from analyses of a million individuals.

rs12777 in MIR3936HG;SLC22A4 gene and RDW - Red blood cell distribution width result PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs12777 in MIR3936HG;SLC22A4 gene and Red cell distribution width determination PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs12777 in MIR3936HG;SLC22A4 gene and fibrinogen activity PMID 20031577 2009 Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.