rs3856806, PPARG

N. diseases: 41
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.
Epithelioma
CUI: C1368683
Disease: Epithelioma
2 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2017 2017
Periodontal Diseases
CUI: C0031090
Disease: Periodontal Diseases
22 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1 2011 2011
Connective Tissue Diseases
CUI: C0009782
Disease: Connective Tissue Diseases
24 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2018 2018
Obesity, Morbid
CUI: C0028756
Disease: Obesity, Morbid
49 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2012 2012
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2004 2004
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2018 2018
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2017 2017
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2017 2017
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2011 2011
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2010 2010
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2018 2018
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1 2012 2012
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.020 1.000 2 2014 2015
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2017 2017
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2015 2015
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2017 2017
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.020 1.000 2 2012 2019
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2011 2011
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2017 2017
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2017 2017
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2017 2017
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1 2013 2013
Squamous cell carcinoma of esophagus
329 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2017 2017
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2019 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.030 1.000 3 2012 2016