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SNP information rs111033566

RS111033566

Normal allele: AA

A novel cationic trypsinogen (PRSS1) cause autosomal dominant hereditary pancreatitis.

Polymorphism rs111033566 is related to topics like this:

Hereditary pancreatitis

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

Research and publications:

  185115   Participation of the beta-receptor system in the genesis of the carotid-aortic baroreceptor reflex in the dog (translated by the author).

  6023921   Hereditary chronic relapsing pancreatitis. A clue to pancreatitis in general?

  9322498   Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis.

  9633818   Mutations of the cationic trypsinogen in hereditary pancreatitis.

  10204851   Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis.

  10835640   Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis.

  10872414   Risk factors for cancer in hereditary pancreatitis. International Hereditary Pancreatitis Study Group.

  10982192   Origin and implication of the hereditary pancreatitis-associated N21I mutation in the cationic trypsinogen gene.

  11719509   Hereditary pancreatitis caused by a novel PRSS1 mutation (Arg-122 --> Cys) that alters autoactivation and autodegradation of cationic trypsinogen.

  11788572   Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis.

  11842279   R116C mutation of cationic trypsinogen in a Turkish family with recurrent pancreatitis illustrates genetic microheterogeneity of hereditary pancreatitis.

  11950817   Mutations in serine protease inhibitor Kazal type 1 are strongly associated with chronic pancreatitis.

  12011155   Mutations in the pancreatic secretory trypsin inhibitor gene (PSTI/SPINK1) rather than the cationic trypsinogen gene (PRSS1) are significantly associated with tropical calcific pancreatitis.

  12853682   The course of genetically determined chronic pancreatitis.

  15028953   Hereditary pancreatitis: clinical characteristics and diagnostic criteria in Japan.

  16632094   Biochemical models of hereditary pancreatitis.

  21415673   High incidence of PRSS1 and SPINK1 mutations in Korean children with acute recurrent and chronic pancreatitis.

  22379635   PRSS1-Related Hereditary Pancreatitis.

  22539344   Increased activation of hereditary pancreatitis-associated human cationic trypsinogen mutants in presence of chymotrypsin C.

  24002981   Comprehensive screening for PRSS1, SPINK1, CFTR, CTRC and CLDN2 gene mutations in Chinese paediatric patients with idiopathic chronic pancreatitis: a cohort study.

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