Variant: rs10479002

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

rs10479002 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.