Variant: rs2158177

present in Gene: TH2LCRR present in Chromosome: 5 Position on Chromosome: 132648366 Alleles of this Variant: A/G

rs2158177 in TH2LCRR gene and Dermatitis, Atopic PMID 23886662 2013 A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis.

rs2158177 in TH2LCRR gene and Fibrinogen assay PMID 20978265 2011 Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe).

rs2158177 in TH2LCRR gene and Fibrinogen, CTCAE PMID 20978265 2011 Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe).

rs2158177 in TH2LCRR gene and fibrinogen activity PMID 20978265 2011 Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe).