Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.870 0.900 1 2006 2020
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.800 1.000 3 2010 2019
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 1 2011 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2016 2019
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0018801
Disease: Heart failure
Heart failure 		0.700 1.000 1 2016 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 1.000 1 2016 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2016 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.700 1.000 1 2016 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0011847
Disease: Diabetes
Diabetes 		0.700 1.000 1 2016 2016
dbSNP: rs4506565
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2016 2016