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SNP information rs4613763

RS4613763

Normal allele: TT

Polymorphism rs4613763 is related to topics like this:

Is multiple sclerosis hereditary disease

The presence of lesions on the brain and spinal cord is indicative of multiple sclerosis, a...

Crohn's disease genetic

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


Research and publications:

  17447842   Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.

  20018022   Replication of recently identified associated single-nucleotide polymorphisms from six autoimmune diseases in Genetic Analysis Workshop 16 rheumatoid arthritis data.

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

  20662065   Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus.

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

  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.

  21487504   Immunopathogenesis of inflammatory bowel disease.

  21533023   Adaptations to climate-mediated selective pressures in humans.

  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.

  21852963   Pervasive sharing of genetic effects in autoimmune disease.

  22164203   Perspectives on the use of multiple sclerosis risk genes for prediction.

  22190364   Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.

  22396755   Genomic regions associated with multiple sclerosis are active in B cells.

  22570697   Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1.

  22770979   Presence of multiple independent effects in risk loci of common complex human diseases.

  23730204   Progress in multiple sclerosis genetics.

  27503178   Effect of autoimmunity risk loci on the honeymoon phase in type 1 diabetes.

  27802296   A Risk Score for Predicting Multiple Sclerosis.

  30568945   Genetic associations of inflammatory bowel disease in a South Asian population.

  32464244   Candidate polymorphisms and susceptibility to inflammatory bowel disease: A systematic review and meta-analysis.

  32846747   Association between PTGER4 polymorphisms and inflammatory bowel disease risk in Caucasian: A meta-analysis.

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

  20222910   Susceptibility loci identified by genome-wide association studies are associated with Crohn's disease in Canadian children.

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

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

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

  23300802   Polymorphisms modulating PTGER4 expression in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites.

Dementia is genetic

Dementia is characterized as a syndrome, rather than a singular disease. Individuals with early...

Alzheimer's disease is hereditary

Alzheimer's disease is a degenerative brain disease that causes dementia, resulting in a gradual...

Is OCD obsessive compulsive disorder genetic

Obsessive-compulsive disorder (OCD) is a mental health condition characterized by features known as...

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