rs1805192, PPARG

N. diseases: 121
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.
BODY MASS INDEX, MODIFIER OF
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
1 0.510 0.840 3 12379739 missense variant C/G snv 0.700 0
DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF
CUI: C4016735
Disease: DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF
1 0.510 0.840 3 12379739 missense variant C/G snv 0.700 0
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
CUI: C1832253
Disease: INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
1 0.510 0.840 3 12379739 missense variant C/G snv 0.700 0
OBESITY, MODIFIER OF
CUI: C1832250
Disease: OBESITY, MODIFIER OF
1 0.510 0.840 3 12379739 missense variant C/G snv 0.700 0
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.510 0.840 3 12379739 missense variant C/G snv 0.100 0.893 103 1997 2018
Obesity
CUI: C0028754
Disease: Obesity
1111 0.510 0.840 3 12379739 missense variant C/G snv 0.100 0.837 43 1997 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.510 0.840 3 12379739 missense variant C/G snv 0.100 0.842 38 1999 2019
Hyperinsulinism
CUI: C0020459
Disease: Hyperinsulinism
64 0.510 0.840 3 12379739 missense variant C/G snv 0.090 1.000 9 1999 2013
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.510 0.840 3 12379739 missense variant C/G snv 0.100 0.813 32 2000 2019
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.510 0.840 3 12379739 missense variant C/G snv 0.040 1.000 4 2000 2012
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.510 0.840 3 12379739 missense variant C/G snv 0.100 0.955 22 2001 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.510 0.840 3 12379739 missense variant C/G snv 0.060 0.667 6 2001 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.510 0.840 3 12379739 missense variant C/G snv 0.050 1.000 5 2001 2010
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.510 0.840 3 12379739 missense variant C/G snv 0.050 1.000 5 2001 2010
Insulin resistance syndrome
CUI: C3714619
Disease: Insulin resistance syndrome
15 0.510 0.840 3 12379739 missense variant C/G snv 0.040 1.000 4 2001 2002
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.510 0.840 3 12379739 missense variant C/G snv 0.020 1.000 2 2001 2014
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2001 2001
obsolete Combined hyperlipidemia
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
4 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2001 2001
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2001 2001
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.510 0.840 3 12379739 missense variant C/G snv 0.100 0.778 18 2002 2013
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.510 0.840 3 12379739 missense variant C/G snv 0.050 0.800 5 2002 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.510 0.840 3 12379739 missense variant C/G snv 0.050 0.800 5 2002 2017
Lipid Metabolism Disorders
CUI: C0154251
Disease: Lipid Metabolism Disorders
10 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2002 2002
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.510 0.840 3 12379739 missense variant C/G snv 0.100 0.800 10 2003 2010
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.510 0.840 3 12379739 missense variant C/G snv 0.060 0.833 6 2003 2016