rs1260326, GCKR

N. diseases: 63
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.
Diabetes
CUI: C0011847
Disease: Diabetes
349 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.010 1.000 1 2011 2011
Fatty Liver
CUI: C0015695
Disease: Fatty Liver
24 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.010 1.000 1 2012 2012
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
37 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.010 1.000 1 2008 2008
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
454 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.010 1.000 1 2011 2011
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
44 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.010 1.000 1 2011 2011
Nonalcoholic Steatohepatitis
CUI: C3241937
Disease: Nonalcoholic Steatohepatitis
11 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.010 1.000 1 2013 2013
Overweight
CUI: C0497406
Disease: Overweight
126 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.010 1.000 1 2016 2016
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
48 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.020 1.000 2 2008 2009
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
440 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.030 1.000 3 2011 2016
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
41 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.030 1.000 3 2012 2016
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
293 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.040 0.750 4 2009 2016
Obesity
CUI: C0028754
Disease: Obesity
811 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.040 1.000 4 2004 2016
Diabetes Mellitus, Non-Insulin-Dependent
1522 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.050 1.000 5 2008 2016
FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5
2 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 4 2008 2010
Creatinine measurement, serum (procedure)
140 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 2 2010 2016
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
956 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 2 2017 2017
Gout
CUI: C0018099
Disease: Gout
90 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 2 2016 2017
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
451 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 2 2016 2017
Amino acids measurement
CUI: C0201874
Disease: Amino acids measurement
42 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2016 2016
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
422 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2017 2017
Aspartate aminotransferase measurement
108 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2011 2011
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
429 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2017 2017
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
284 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2017 2017
Cholecystolithiasis
CUI: C0947622
Disease: Cholecystolithiasis
58 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2017 2017
Cholelithiasis
CUI: C0008350
Disease: Cholelithiasis
65 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2017 2017