rs8192678, PPARGC1A

N. diseases: 28
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
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.100 0.879 33 2001 2020
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.100 1.000 14 2003 2015
Obesity
CUI: C0028754
Disease: Obesity
1111 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.080 0.875 8 2003 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.060 0.833 6 2004 2018
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.050 0.800 5 2004 2018
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.040 0.750 4 2005 2020
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.030 1.000 3 2008 2016
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.030 1.000 3 2013 2017
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.030 1.000 3 2010 2018
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.020 0.500 2 2004 2014
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.020 0.500 2 2007 2017
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.020 1.000 2 2004 2005
Metabolic Diseases
CUI: C0025517
Disease: Metabolic Diseases
50 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.020 1.000 2 2006 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.020 0.500 2 2011 2018
Angina, Unstable
CUI: C0002965
Disease: Angina, Unstable
21 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.010 1.000 1 2019 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.010 1.000 1 2019 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.010 1.000 1 2016 2016
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.010 1.000 1 2010 2010
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.010 1 2005 2005
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.010 1.000 1 2016 2016
Hyperinsulinism
CUI: C0020459
Disease: Hyperinsulinism
64 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.010 1.000 1 2010 2010
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.010 1.000 1 2007 2007
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.010 1.000 1 2012 2012
Left ventricular diastolic dysfunction
CUI: C1273070
Disease: Left ventricular diastolic dysfunction
1 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.010 1.000 1 2008 2008
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 0.010 1.000 1 2014 2014