rs290487, TCF7L2

N. diseases: 10
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 Mellitus, Non-Insulin-Dependent
2672 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.100 0.667 15 2007 2015
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.020 0.500 2 2010 2012
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.010 1.000 1 2016 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.010 1.000 1 2016 2016
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.010 1.000 1 2018 2018
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.010 1.000 1 2016 2016
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.010 1.000 1 2020 2020
Impaired insulin secretion
CUI: C0948379
Disease: Impaired insulin secretion
14 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.010 1.000 1 2012 2012
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.010 1.000 1 2013 2013
Obesity
CUI: C0028754
Disease: Obesity
1111 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.010 1.000 1 2016 2016