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.
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2010 2010
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2005 2005
CATARACT, ANTERIOR POLAR
CUI: C1855179
Disease: CATARACT, ANTERIOR POLAR
27 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2014 2014
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1 2016 2016
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2016 2016
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2010 2010
Complications of Diabetes Mellitus
CUI: C0342257
Disease: Complications of Diabetes Mellitus
35 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1 2006 2006
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1 2019 2019
Connective Tissue Diseases
CUI: C0009782
Disease: Connective Tissue Diseases
24 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2018 2018
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
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
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
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2004 2004
Exophthalmos
CUI: C0015300
Disease: Exophthalmos
12 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2009 2009
Fatty Liver, Alcoholic
CUI: C0015696
Disease: Fatty Liver, Alcoholic
6 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2010 2010
Finding of body mass index
CUI: C0578022
Disease: Finding of body mass index
252 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.700 1.000 1 2012 2012
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
Gastrointestinal Diseases
CUI: C0017178
Disease: Gastrointestinal Diseases
14 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2010 2010
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2009 2009
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1 2019 2019
Heart Failure, Diastolic
CUI: C1135196
Disease: Heart Failure, Diastolic
9 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2017 2017
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2018 2018
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2014 2014