rs199769221, PRSS1

N. diseases: 8
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
0.040 GeneticVariation BEFREE The Arg(117) --> His substitution is believed to cause pancreatitis by stabilizing trypsin against autolytic degradation, while the mechanism of action of Asn(21) --> Ile has been unknown. 10514442 1999
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
0.040 GeneticVariation BEFREE The Arg117-->His substitution is believed to cause pancreatitis by eliminating an essential autolytic cleavage site in trypsin, thereby rendering the protease resistant to inactivation through autolysis. 10529393 1999
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
0.040 GeneticVariation BEFREE Unlike in patients with hereditary pancreatitis, we found a lack of the R117H mutation in the cationic trypsinogen gene in all patients with tropical pancreatitis from Bangladesh. 9788542 1998
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
0.040 GeneticVariation BEFREE We recently identified a single R117H mutation in the cationic trypsinogen gene in several kindreds with an inherited form of acute and chronic pancreatitis (HP1), providing strong evidence that trypsin plays a central role in premature zymogen activation and pancreatitis. 9322498 1997