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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2017 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2017 2017
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2016 2016
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2016 2016
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.020 0.500 2 2014 2016
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2013 2013
Lipodystrophy
CUI: C0023787
Disease: Lipodystrophy
28 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1 2012 2012
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2011 2011
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2011 2011
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2009 2009
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
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
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