rs1801282, PPARG

N. diseases: 131
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 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.900 0.902 122 1997 2018
Obesity
CUI: C0028754
Disease: Obesity
1111 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.100 0.804 46 1997 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.100 0.842 38 1999 2018
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.100 0.813 32 2000 2014
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.100 0.960 25 2001 2018
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.100 0.789 19 2002 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.100 0.846 13 2003 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.100 0.917 12 2005 2015
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.100 0.800 10 2004 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.090 0.778 9 2005 2013
Hyperinsulinism
CUI: C0020459
Disease: Hyperinsulinism
64 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.090 1.000 9 1999 2013
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.090 0.778 9 2010 2014
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.080 1.000 8 2008 2019
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.080 1.000 8 2008 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.070 0.857 7 2002 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.070 0.714 7 2001 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.070 0.857 7 2002 2018
Malignant neoplasm of colon and/or rectum
502 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.070 1.000 7 2005 2010
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.070 1.000 7 2001 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.070 1.000 7 2001 2014
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.060 0.500 6 2005 2015
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.060 0.833 6 2003 2015
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.060 1.000 6 2005 2012
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.060 0.667 6 2007 2012
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.060 1.000 6 2008 2019