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SNP information rs3764147

RS3764147

Normal allele: AA

Polymorphism rs3764147 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.

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

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

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

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

  21102463   Genome-wide meta-analysis increases the number of confirmed susceptibility loci for Crohn's disease to 71.

  21119019   Leprosy and the human genome.

  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.

  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.

  22220182   Human polymorphisms as clinical predictors in leprosy.

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

  23974994   Replication study of ulcerative colitis risk loci in a Lithuanian-Latvian case-control sample.

  26235265   Association between genetic variants in NOD2, C13orf31, and CCDC122 genes and leprosy among the Chinese Yi population.

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

  27219008   Pauci- and Multibacillary Leprosy: Two Distinct, Genetically Neglected Diseases.

  27538955   Network or regression-based methods for disease discrimination: a comparison study.

  29706348   Missense Variants in HIF1A and LACC1 Contribute to Leprosy Risk in Han Chinese.

  32421744   Family-based genome-wide association study of leprosy in Vietnam.

  34285550   Single-Nucleotide Polymorphisms Related to Leprosy Risk and Clinical Phenotypes Among Chinese Population.

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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