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SNP information rs4263839

RS4263839

Normal allele: GG

Polymorphism rs4263839 is related to topics like this:

Crohn's disease genetic

A chronic disorder known as Crohn's disease is a multi-faceted condition that primarily impacts the...


Research and publications:

  18587394   Genome-wide association identifies more than 30 different susceptibility loci for Crohn's disease.

  19557189   Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions

  20176734   Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects.

  20228799   Genome-wide association identifies multiple ulcerative colitis susceptibility loci.

  20805105   Synthetic associations in the context of genome-wide association scan signals

  21152001   The association of 1q32 and STAT3 variants with ankylosing spondylitis suggests genetic overlap with Crohn's disease.

  21217814   Presymptomatic risk assessment for chronic non-communicable diseases.

  21304977   An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.

  21487504   Immunopathogenesis of inflammatory bowel disease.

  21548950   Evaluation of 22 genetic variants with risk for Crohn's disease in an Ashkenazi Jewish population: a case-control study.

  21636646   Association of TNFSF15 polymorphism with irritable bowel syndrome.

  21730793   The influence of risk alleles for Crohn's disease and smoking on the location of the disease.

  21752155   Genetic susceptibility to inflammation and colonic transit in lower functional gastrointestinal disorders: preliminary analysis.

  21818367   Investigation of multiple susceptibility loci for inflammatory bowel disease in an Italian cohort of patients.

  21830272   Different and overlapping genetic loci in Crohn's disease and ulcerative colitis: correlation with pathogenesis.

  22127647   A novel bayesian graphical model for genome-wide multi-SNP association mapping.

  23300620   Genotype/phenotype analysis of 53 genetic polymorphisms associated with Crohn's disease.

  25012842   Genetic variation in GPBAR1 predisposes to quantitative changes in colonic transit and bile acid excretion.

  25028192   Association between TNFSF15 polymorphism and susceptibility to ulcerative colitis and Crohn's disease: a meta-analysis.

  25061809   Analyzing genome-wide association studies with an FDR controlling modification of the Bayesian Information Criterion.

  25501099   Protective association of tumor necrosis factor superfamily 15 (TNFSF15) polymorphic haplotype with ulcerative colitis and Crohn's disease in an Indian population.

  25548468   Genetic polymorphism in pathogenesis of irritable bowel syndrome.

  25824902   A meta-analysis of immunogenetic Case-Control Association Studies in irritable bowel syndrome.

  27156530   Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility.

  27336838   Blood and gut eQTLs from an anti-TNF-resistant Crohn's disease cohort inform genetic association loci for IBD.

  27417569   Systematic review: genetic biomarkers associated with anti-TNF treatment response in inflammatory bowel diseases.

  27507062   Fine mapping analysis revealed a complex pleiotropic effect and tissue-specific regulatory mechanism of TNFSF15 in primary biliary cholangitis, Crohn's disease and leprosy.

  27647972   A case-control study about the association between vascular endothelial growth inhibitor gene polymorphisms and breast cancer risk in female patients in Northeast China.

  27892471   Combining Multiple Hypothesis Testing with Machine Learning Increases the Statistical Power of Genome-wide Association Studies.

  28624054   Diverticulitis and Crohn's disease have separate but overlapping tumor necrosis superfamily 15Â haplotypes.

  29446656   Crohn's disease candidate gene alleles predict time to progression from the B1 inflammatory phenotype to the stricturing B2 or penetrating B3 phenotype.

  31052430   Genetic Studies of Inflammatory Bowel Disease-Focusing on Asian Patients.

  31615448   Candidate single nucleotide polymorphisms of irritable bowel syndrome: a systemic review and meta-analysis.

  35207633   The Associations of Single Nucleotide Polymorphisms with Risk and Symptoms of Irritable Bowel Syndrome.

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