rs780094, GCKR

N. diseases: 62
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.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.010 1.000 1 2012 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.010 1.000 1 2018 2018
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.010 1.000 1 2014 2014
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.010 1.000 1 2014 2014
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.010 1.000 1 2018 2018
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.010 1.000 1 2012 2012
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.010 1.000 1 2012 2012
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.010 1.000 1 2015 2015
Nonalcoholic Steatohepatitis
CUI: C3241937
Disease: Nonalcoholic Steatohepatitis
17 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.010 1.000 1 2014 2014
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.010 1.000 1 2012 2012
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.010 1.000 1 2017 2017
Spina Bifida
CUI: C0080178
Disease: Spina Bifida
61 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.010 1.000 1 2015 2015
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 2 2008 2015
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 2 2009 2015
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.710 1.000 2 2010 2016
Fatty Liver
CUI: C0015695
Disease: Fatty Liver
35 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.020 1.000 2 2013 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.810 1.000 3 2010 2016
Body mass index
CUI: C1305855
Disease: Body mass index
2689 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 3 2012 2019
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 3 2008 2019
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 3 2011 2018
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 3 2011 2018
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 3 2008 2019
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.030 1.000 3 2008 2018
Obesity
CUI: C0028754
Disease: Obesity
1111 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.030 1.000 3 2009 2018
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.030 1.000 3 2013 2018