rs11554495, KRT8

N. diseases: 19
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.
Cirrhosis, Cryptogenic
CUI: C0267809
Disease: Cirrhosis, Cryptogenic
5 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.700 0
Cirrhosis, Familial
CUI: C1861556
Disease: Cirrhosis, Familial
6 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.700 0
CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO (finding)
CUI: C1835713
Disease: CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO (finding)
2 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.700 0
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.020 0.500 2 2004 2014
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.020 1.000 2 2003 2006
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
80 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.020 1.000 2 2006 2006
Pancreatitis, Chronic
CUI: C0149521
Disease: Pancreatitis, Chronic
56 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.020 1.000 2 2003 2006
Acute on chronic pancreatitis
CUI: C0262417
Disease: Acute on chronic pancreatitis
7 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.010 1.000 1 2006 2006
Alcoholic Liver Diseases
CUI: C0023896
Disease: Alcoholic Liver Diseases
20 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.010 1.000 1 2006 2006
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.010 1.000 1 2003 2003
Colon adenoma
CUI: C4551463
Disease: Colon adenoma
1 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.010 1.000 1 2006 2006
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.010 1.000 1 2004 2004
Hereditary pancreatitis
CUI: C0238339
Disease: Hereditary pancreatitis
108 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.010 1.000 1 2006 2006
Iron Overload
CUI: C0282193
Disease: Iron Overload
53 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.010 1.000 1 2012 2012
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.010 1.000 1 2006 2006
Liver Failure, Acute
CUI: C0162557
Disease: Liver Failure, Acute
21 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.010 1.000 1 2015 2015
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.010 1.000 1 2006 2006
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.010 1.000 1 2006 2006
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 0.010 1.000 1 2004 2004