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SNP information rs212388

RS212388

Normal allele: CC

Polymorphism rs212388 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:

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

  21298027   Meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as common risk loci for Crohn's disease and celiac disease.

  21383967   Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.

  23044675   TAGAP mutation protects against anal sepsis in ileocolic Crohn's disease.

  24582067   T cell activation. Expression of Rho-GTPase activating protein varies depending on the location and severity of inflammation in Crohn's disease.

  24999842   Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.

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

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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