rs266729, ADIPOQ

N. diseases: 37
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.
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.100 1.000 14 2009 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.060 0.833 6 2008 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.060 0.833 6 2011 2019
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.060 1.000 6 2010 2019
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.060 1.000 6 2010 2017
Obesity
CUI: C0028754
Disease: Obesity
1111 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.050 1.000 5 2013 2020
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.040 1.000 4 2010 2017
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.040 0.750 4 2008 2017
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.040 0.500 4 2013 2017
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.040 1.000 4 2015 2020
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.040 0.500 4 2013 2017
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.030 0.333 3 2011 2018
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.030 1.000 3 2010 2015
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.030 0.667 3 2006 2015
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.020 1.000 2 2011 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.020 1.000 2 2011 2011
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.020 1.000 2 2011 2012
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.020 1.000 2 2009 2015
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.020 1.000 2 2011 2019
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.010 1.000 1 2017 2017
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.010 1.000 1 2008 2008
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.010 1.000 1 2011 2011
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.010 1.000 1 2015 2015
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.010 1.000 1 2009 2009
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.010 1.000 1 2011 2011