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.
Glomerular Filtration Rate
CUI: C0017654
Disease: Glomerular Filtration Rate
1033 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2019 2019
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.010 1.000 1 2018 2018
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
Glucose tolerance test
CUI: C0017741
Disease: Glucose tolerance test
28 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2018 2018
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
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.040 1.000 4 2017 2018
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
535 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2017 2017
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
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
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2016 2016
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2016 2016
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2016 2016
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
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
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