rs10865710, PPARG

N. diseases: 13
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.
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.700 1.000 1 2017 2017
Associated Pulmonary Arterial Hypertension
4 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2015 2015
Asthma
CUI: C0004096
Disease: Asthma
1536 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2017 2017
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2016 2016
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2009 2009
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2017 2017
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2014 2014
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2012 2012
Obesity
CUI: C0028754
Disease: Obesity
1111 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2018 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2014 2014
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2016 2016
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2016 2016
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2015 2015