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.
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2011 2011
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 4 2012 2019
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
Body mass index procedure
CUI: C0005893
Disease: Body mass index procedure
252 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2012 2012
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
Fasting blood sugar result
CUI: C1261430
Disease: Fasting blood sugar result
113 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2012 2012
Finding of body mass index
CUI: C0578022
Disease: Finding of body mass index
252 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2012 2012
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
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
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2012 2012
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
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
Calcium level result
CUI: C0428302
Disease: Calcium level result
51 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2013 2013
Calcium measurement
CUI: C0201925
Disease: Calcium measurement
71 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 1 2013 2013
Body Height
CUI: C0005890
Disease: Body Height
3972 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2014 2014
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
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
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
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
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2016 2016
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2016 2016
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2016 2016
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2016 2016