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.
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.030 1.000 3 2007 2019
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.020 1.000 2 2007 2012
Metabolic Diseases
CUI: C0025517
Disease: Metabolic Diseases
50 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.020 1.000 2 2007 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
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
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.050 1.000 5 2008 2014
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.040 0.750 4 2008 2012
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
121 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.040 1.000 4 2008 2019
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.030 1.000 3 2008 2008
Infection caused by Helicobacter pylori
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
56 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.020 1.000 2 2008 2010
Kidney Failure
CUI: C0035078
Disease: Kidney Failure
36 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.020 1.000 2 2008 2015
Peptic Ulcer
CUI: C0030920
Disease: Peptic Ulcer
25 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.020 1.000 2 2008 2010
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2008 2008
Sarcoidosis
CUI: C0036202
Disease: Sarcoidosis
787 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2008 2008
Pediatric Obesity
CUI: C2362324
Disease: Pediatric Obesity
67 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.030 1.000 3 2009 2018
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.020 2 2009 2015
Lipodystrophy
CUI: C0023787
Disease: Lipodystrophy
28 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.020 0.500 2 2009 2014
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.020 1.000 2 2009 2014
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.020 1.000 2 2009 2014
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2009 2009
Asthma
CUI: C0004096
Disease: Asthma
1536 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2009 2009
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2009 2009
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2009 2009
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2009 2009