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SNP information rs11584383

RS11584383

Normal allele: TT

Polymorphism rs11584383 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:

  20007504   Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci.

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

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

  21217814   Presymptomatic risk assessment for chronic non-communicable diseases.

  21297633   Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.

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

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

  21852963   Pervasive sharing of genetic effects in autoimmune disease.

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

  27936930   Different Contributions of CDKAL1, KIF21B, and LRRK2/MUC19 Polymorphisms to SAPHO Syndrome, Rheumatoid Arthritis, Ankylosing Spondylitis, and Seronegative Spondyloarthropathy.

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

  19068216   Investigation of Crohn's disease risk loci in ulcerative colitis further determines their molecular relatedness.

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

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

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

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

  29967744   Association of Crohn's disease-associated chromosome 1q32 with ankylosing spondylitis is independent of bowel symptoms and fecal calprotectin.

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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