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SNP information rs2188962

RS2188962

Normal allele: CC

Polymorphism rs2188962 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.

  19408013   Strategies and issues in the detection of pathway enrichment in genome-wide association studies

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

  20014019   Genome wide association (GWA) predictors of anti-TNFalpha therapeutic responsiveness in pediatric inflammatory bowel disease.

  20031576   Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.

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

  20369022   Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.

  20570966   Nonsecretory fucosyltransferase 2 (FUT2) status is associated with Crohn's disease.

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

  20833654   Mapping of numerous disease-associated expression polymorphisms in primary peripheral blood CD4+ lymphocytes.

  20923970   Bayesian epistasis association mapping via SNP imputation.

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

  21333900   The role of genetics in IBS

  21487504   Immunopathogenesis of inflammatory bowel disease.

  21674708   Two independent genetic factors are responsible for the association of the IBD5 locus with Crohn's disease in the Czech population.

  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.

  21852963   Pervasive sharing of genetic effects in autoimmune disease.

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

  23818875   DeepSAGE reveals genetic variants associated with alternative polyadenylation and expression of coding and non-coding transcripts.

  26821299   Genetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease.

  27153397   Mechanisms and Disease Associations of Haplotype-Dependent Allele-Specific DNA Methylation.

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

  27274049   Early farmers from across Europe directly descended from Neolithic Aegeans.

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

  31469255   A genome-wide association and replication study of blood pressure in Ugandan early adolescents.

Is rheumatoid arthritis genetic

Chronic abnormal inflammation is the hallmark of rheumatoid arthritis, a disease that primarily...

Hereditary pancreatitis

Pancreatitis is a multifaceted ailment that can stem from various sources. If pancreatitis arises...

Heart attack genetic

Genetic predisposition, also referred to as familial predisposition, is a crucial risk factor for...

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