SNP information rs111033565
Normal allele: GG
rs111033565(A) is the most common mutation found in early (childhood) acute recurrent pancreatitis or chronic pancreatitis.
Polymorphism rs111033565 is related to topics like this:
Pancreatitis is a multifaceted ailment that can stem from various sources. If pancreatitis arises...
Research and publications:
1720414 Monoclonal antibodies which identify carbohydrate-defined MHC class I epitopes.
8841182 Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene.
9557894 Heterogeneity in hereditary pancreatitis.
10909845 Molecular basis of hereditary pancreatitis.
12413370 Spontaneous and sporadic trypsinogen mutations in idiopathic pancreatitis.
16791840 Mutations of human cationic trypsinogen (PRSS1) and chronic pancreatitis.
16885867 Estimation of the prevalence and incidence of chronic pancreatitis and its complications.
18286680 Role of genetic disorders in acute recurrent pancreatitis.
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