rs1260326, GCKR

N. diseases: 81
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.
Lactic acid measurement
CUI: C0202115
Disease: Lactic acid measurement
2 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2016 2016
FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5
2 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 0
Serum total protein measurement
CUI: C0036836
Disease: Serum total protein measurement
6 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2012 2012
Insulin C-peptide measurement
CUI: C0202100
Disease: Insulin C-peptide measurement
7 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2013 2013
Serum albumin level
CUI: C0728877
Disease: Serum albumin level
9 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2012 2012
Nonalcoholic Steatohepatitis
CUI: C3241937
Disease: Nonalcoholic Steatohepatitis
17 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.010 1.000 1 2014 2014
Monogenic diabetes
CUI: C3888631
Disease: Monogenic diabetes
19 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.010 1.000 1 2014 2014
Glucose tolerance test
CUI: C0017741
Disease: Glucose tolerance test
28 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 1 2010 2010
Biliary calculi
CUI: C0242216
Disease: Biliary calculi
31 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 2 2016 2018
Urolithiasis
CUI: C0451641
Disease: Urolithiasis
33 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2019 2019
Fatty Liver
CUI: C0015695
Disease: Fatty Liver
35 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.020 1.000 2 2012 2018
Factor VII measurement
CUI: C2825856
Disease: Factor VII measurement
36 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2019 2019
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
53 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2009 2009
Sodium measurement
CUI: C0337443
Disease: Sodium measurement
69 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2019 2019
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.040 1.000 4 2012 2018
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.020 1.000 2 2013 2014
Amino acids measurement
CUI: C0201874
Disease: Amino acids measurement
92 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 2 2016 2016
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.010 1.000 1 2011 2011
Serum gamma-glutamyl transferase measurement
108 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 2 2011 2018
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.010 1.000 1 2008 2008
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 2 2009 2018
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 2 2009 2018
Fasting blood sugar result
CUI: C1261430
Disease: Fasting blood sugar result
113 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2012 2012
RESTING HEART RATE
CUI: C1821417
Disease: RESTING HEART RATE
134 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 2 2016 2018
Granulocyte count
CUI: C0857490
Disease: Granulocyte count
150 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2016 2016