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
CUI: C0011860
Disease: 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
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
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
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.040 1.000 4 2000 2012
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
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 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
Insulin resistance syndrome
CUI: C3714619
Disease: Insulin resistance syndrome
15 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.040 1.000 4 2001 2002
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2001 2001
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2001 2001
obsolete Combined hyperlipidemia
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
4 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2001 2001
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2001 2001
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
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
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
Lipid Metabolism Disorders
CUI: C0154251
Disease: Lipid Metabolism Disorders
10 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.020 1.000 2 2002 2016
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
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
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.050 0.600 5 2003 2015
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.030 1.000 3 2003 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.030 1.000 3 2003 2014
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.030 0.667 3 2003 2015