rs267606982, PRSS1

N. diseases: 11
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hereditary pancreatitis
CUI: C0238339
Disease: Hereditary pancreatitis
108 0.742 0.120 7 142751938 missense variant GC/AT mnv 0.900 1.000 26 1996 2012
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
80 0.742 0.120 7 142751938 missense variant GC/AT mnv 0.100 0.800 10 2000 2020
Pancreatitis, Chronic
CUI: C0149521
Disease: Pancreatitis, Chronic
56 0.742 0.120 7 142751938 missense variant GC/AT mnv 0.060 1.000 6 2001 2017
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.742 0.120 7 142751938 missense variant GC/AT mnv 0.030 1.000 3 2006 2012
Idiopathic chronic pancreatitis
CUI: C0341471
Disease: Idiopathic chronic pancreatitis
16 0.742 0.120 7 142751938 missense variant GC/AT mnv 0.030 1.000 3 2001 2017
Autosomal Dominant Hereditary Pancreatitis
6 0.742 0.120 7 142751938 missense variant GC/AT mnv 0.020 1.000 2 2006 2010
Acute on chronic pancreatitis
CUI: C0262417
Disease: Acute on chronic pancreatitis
7 0.742 0.120 7 142751938 missense variant GC/AT mnv 0.010 1.000 1 2003 2003
Hyperparathyroidism, Primary
CUI: C0221002
Disease: Hyperparathyroidism, Primary
39 0.742 0.120 7 142751938 missense variant GC/AT mnv 0.010 1.000 1 2008 2008
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.742 0.120 7 142751938 missense variant GC/AT mnv 0.010 1.000 1 2008 2008
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.742 0.120 7 142751938 missense variant GC/AT mnv 0.010 1.000 1 2008 2008
Recurrent pancreatitis
CUI: C4551632
Disease: Recurrent pancreatitis
13 0.742 0.120 7 142751938 missense variant GC/AT mnv 0.010 1.000 1 2012 2012