Variant: rs3131296 

    present in Gene: NOTCH4
    present in Chromosome: 6
    Position on Chromosome: 32205216
    Alleles of this Variant: C/T

rs3131296 in NOTCH4 gene and Diabetes Mellitus, Insulin-Dependent PMID 17632545 2007 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.

rs3131296 in NOTCH4 gene and Lupus Erythematosus, Systemic PMID 24871463 2014 GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region.

rs3131296 in NOTCH4 gene and Myasthenia Gravis PMID 23055271 2012 Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.

rs3131296 in NOTCH4 gene and Rheumatoid Arthritis PMID 19503088 2009 REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.

PMID 21156761 2011 A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis.

PMID 17804836 2007 TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.

rs3131296 in NOTCH4 gene and Schizophrenia PMID 19571808 2009 Common variants conferring risk of schizophrenia.

PMID 21791550 2011 Common variants at VRK2 and TCF4 conferring risk of schizophrenia.

rs3131296 in NOTCH4 gene and Vitiligo PMID 20526339 2010 Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC.