rs7903146, TCF7L2

N. diseases: 93
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.
Insulin measurement
CUI: C0202098
Disease: Insulin measurement
25 0.554 0.680 10 112998590 intron variant C/G;T snv 0.800 1.000 1 2011 2011
Autoantibody measurement
CUI: C1272321
Disease: Autoantibody measurement
52 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2009 2009
Birth Weight
CUI: C0005612
Disease: Birth Weight
369 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2019 2019
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2017 2017
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2017 2017
Glycosuria
CUI: C0017979
Disease: Glycosuria
7 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2019 2019
Hip circumference
CUI: C0562350
Disease: Hip circumference
116 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2015 2015
Physical Activity Measurement
CUI: C4049938
Disease: Physical Activity Measurement
355 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2017 2017
Smoking
CUI: C0037369
Disease: Smoking
765 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2017 2017
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2019 2019
Waist Circumference
CUI: C0455829
Disease: Waist Circumference
183 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2015 2015
Adenocarcinoma of the gastroesophageal junction
CUI: C1332166
Disease: Adenocarcinoma of the gastroesophageal junction
6 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2019 2019
Atherogenic dyslipidaemia
CUI: C4524040
Disease: Atherogenic dyslipidaemia
9 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2009 2009
Autonomic neuropathy
CUI: C0259749
Disease: Autonomic neuropathy
7 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2013 2013
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2018 2018
Cholangiocarcinoma
CUI: C0206698
Disease: Cholangiocarcinoma
43 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2017 2017
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2014 2014
Constitutional obesity
CUI: C2937224
Disease: Constitutional obesity
3 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2008 2008
Cystic Fibrosis
CUI: C0010674
Disease: Cystic Fibrosis
704 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2009 2009
Diabetes in youth
CUI: C3825462
Disease: Diabetes in youth
2 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2011 2011
Diabetic foot ulcer
CUI: C1456868
Disease: Diabetic foot ulcer
17 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2013 2013
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2015 2015
Familial obesity
CUI: C1281440
Disease: Familial obesity
3 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2008 2008
Glioma
CUI: C0017638
Disease: Glioma
353 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2018 2018
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2015 2015