Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10865710
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2014 2014
dbSNP: rs10865710
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2017 2017
dbSNP: rs10865710
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2018 2018
dbSNP: rs10865710
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0036690
Disease: Septicemia
Septicemia 		0.010 1.000 1 2016 2016
dbSNP: rs10865710
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0243026
Disease: Sepsis
Sepsis 		0.010 1.000 1 2016 2016
dbSNP: rs10865710
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2014 2014
dbSNP: rs10865710
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		0.010 1.000 1 2009 2009
dbSNP: rs10865710
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2017 2017
dbSNP: rs10865710
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C1701938
Disease: Associated Pulmonary Arterial Hypertension
Associated Pulmonary Arterial Hypertension 		0.010 1.000 1 2015 2015
dbSNP: rs10865710
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.010 1.000 1 2015 2015
dbSNP: rs10865710
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		0.010 1.000 1 2012 2012
dbSNP: rs10865710
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.010 1.000 1 2016 2016
dbSNP: rs1151996
rs1151996
PPARG
1.000 0.120 3 12404308 intron variant C/A snv 0.70
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.010 1.000 1 2018 2018
dbSNP: rs1151999
rs1151999
PPARG
1.000 0.080 3 12405654 intron variant G/T snv 0.61
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2011 2011
dbSNP: rs11715073
rs11715073
PPARG
0.925 0.120 3 12311472 intron variant C/G snv 0.25
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2010 2010
dbSNP: rs1175543
rs1175543
PPARG
0.851 0.120 3 12424934 intron variant A/G snv 0.28
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2008 2008
dbSNP: rs1175543
rs1175543
PPARG
0.851 0.120 3 12424934 intron variant A/G snv 0.28
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 < 0.001 1 2018 2018
dbSNP: rs1175543
rs1175543
PPARG
0.851 0.120 3 12424934 intron variant A/G snv 0.28
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2014 2014
dbSNP: rs1175543
rs1175543
PPARG
0.851 0.120 3 12424934 intron variant A/G snv 0.28
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2008 2008
dbSNP: rs1175543
rs1175543
PPARG
0.851 0.120 3 12424934 intron variant A/G snv 0.28
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2008 2008
dbSNP: rs121909244
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 1.000 1 2005 2005
dbSNP: rs121909244
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		0.010 1.000 1 2010 2010
dbSNP: rs121909244
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2004 2004
dbSNP: rs121909244
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2005 2005
dbSNP: rs121909244
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06
CUI: C4316789
Disease: Partial lipodystrophy
Partial lipodystrophy 		0.010 1.000 1 2005 2005