rs1805192, PPARG

N. diseases: 121
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.
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2008 2008
Gastrointestinal Diseases
CUI: C0017178
Disease: Gastrointestinal Diseases
14 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2010 2010
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2009 2009
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1 2019 2019
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2014 2014
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2014 2014
Human immunodeficiency virus (HIV) II infection category B1
CUI: C3854222
Disease: Human immunodeficiency virus (HIV) II infection category B1
56 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2014 2014
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2014 2014
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1 2011 2011
Lipid Metabolism Disorders
CUI: C0154251
Disease: Lipid Metabolism Disorders
10 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2002 2002
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2009 2009
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2016 2016
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2004 2004
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2009 2009
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2005 2005
Mental Depression
CUI: C0011570
Disease: Mental Depression
271 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2009 2009
Metabolic Diseases
CUI: C0025517
Disease: Metabolic Diseases
50 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2007 2007
metabolic disturbance
CUI: C0746556
Disease: metabolic disturbance
4 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2014 2014
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2009 2009
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2019 2019
Obesity, Morbid
CUI: C0028756
Disease: Obesity, Morbid
49 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2012 2012
obsolete Combined hyperlipidemia
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
4 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2001 2001
Obstructive sleep apnea hypopnea syndrome
CUI: C4285910
Disease: Obstructive sleep apnea hypopnea syndrome
7 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1 2011 2011
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2009 2009
Premature adrenarche
CUI: C0342546
Disease: Premature adrenarche
11 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2010 2010