rs17107315, SPINK1

N. diseases: 40
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.
Pancreatic adenocarcinoma metastatic
2 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1.000 1 2017 2017
Idiopathic bronchiectasis
CUI: C0339985
Disease: Idiopathic bronchiectasis
6 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1.000 1 2014 2014
Annular pancreas
CUI: C0149955
Disease: Annular pancreas
1 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1.000 1 2013 2013
Obstructive chronic pancreatitis
CUI: C0341472
Disease: Obstructive chronic pancreatitis
1 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1.000 1 2013 2013
Recurrent pancreatitis
CUI: C4551632
Disease: Recurrent pancreatitis
13 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1.000 1 2012 2012
Exocrine pancreatic insufficiency
CUI: C0267963
Disease: Exocrine pancreatic insufficiency
26 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.020 1.000 2 2011 2019
pancreatitis idiopathic
CUI: C0747198
Disease: pancreatitis idiopathic
4 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.020 1.000 2 2011 2011
Congenital bilateral aplasia of vas deferens
210 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1.000 1 2011 2011
Pancreatic Insufficiency
CUI: C0030293
Disease: Pancreatic Insufficiency
23 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1.000 1 2011 2011
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1.000 1 2009 2009
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1.000 1 2009 2009
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1.000 1 2009 2009
Hyperparathyroidism, Primary
CUI: C0221002
Disease: Hyperparathyroidism, Primary
39 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.020 1.000 2 2008 2011
Acute recurrent pancreatitis
CUI: C0267937
Disease: Acute recurrent pancreatitis
7 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.060 0.667 6 2006 2014
Hypocalciuric hypercalcemia, familial, type 1
58 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1.000 1 2006 2006
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.080 0.875 8 2005 2015
Pancreatitis, Alcoholic
CUI: C0376670
Disease: Pancreatitis, Alcoholic
86 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1 2005 2005
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.020 1.000 2 2004 2019
Pancreatitis, Calcific
CUI: C1868653
Disease: Pancreatitis, Calcific
2 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.020 1.000 2 2004 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.020 1.000 2 2004 2019
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1.000 1 2004 2004
Pancreatic carcinoma, familial
CUI: C2931038
Disease: Pancreatic carcinoma, familial
9 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1.000 1 2004 2004
Parotitis
CUI: C0030583
Disease: Parotitis
2 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.010 1 2004 2004
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.040 0.750 4 2003 2007
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.040 0.750 4 2003 2007