rs1800206, PPARA

N. diseases: 35
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.
HYPERAPOBETALIPOPROTEINEMIA, SUSCEPTIBILITY TO
1 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.700 0
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.070 0.857 7 2000 2013
Obesity
CUI: C0028754
Disease: Obesity
1111 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.060 0.667 6 2001 2016
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.020 1.000 2 2001 2013
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.020 1.000 2 2002 2004
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.020 1.000 2 2002 2004
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2002 2002
Lipid Metabolism Disorders
CUI: C0154251
Disease: Lipid Metabolism Disorders
10 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2002 2002
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2002 2002
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.020 1.000 2 2003 2009
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.030 1.000 3 2004 2016
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.030 0.667 3 2004 2014
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.030 1.000 3 2004 2015
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.020 0.500 2 2004 2012
Dystrophia myotonica 2
CUI: C2931689
Disease: Dystrophia myotonica 2
21 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2004 2004
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.040 0.750 4 2005 2007
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.030 0.667 3 2005 2007
Fatty Liver
CUI: C0015695
Disease: Fatty Liver
35 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2005 2005
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2005 2005
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2005 2005
Nonalcoholic Steatohepatitis
CUI: C3241937
Disease: Nonalcoholic Steatohepatitis
17 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2005 2005
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2005 2005
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2008 2008
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1 2008 2008
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2008 2008