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.
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2017 2017
Asthma
CUI: C0004096
Disease: Asthma
1536 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2015 2015
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.597 0.720 3 186853334 intron variant G/C;T snv 0.030 1.000 3 2008 2013
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2014 2014
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.597 0.720 3 186853334 intron variant G/C;T snv 0.050 0.600 5 2011 2018
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2012 2012
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2012 2012
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.597 0.720 3 186853334 intron variant G/C;T snv 0.040 0.750 4 2014 2015
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.597 0.720 3 186853334 intron variant G/C;T snv 0.030 1.000 3 2012 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.597 0.720 3 186853334 intron variant G/C;T snv 0.090 1.000 9 2012 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.597 0.720 3 186853334 intron variant G/C;T snv 0.070 1.000 7 2012 2018
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2015 2015
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2015 2015
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2017 2017
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2017 2017
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.597 0.720 3 186853334 intron variant G/C;T snv 0.100 0.923 13 2009 2019
Diabetic dyslipidaemia
CUI: C3160761
Disease: Diabetic dyslipidaemia
11 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2017 2017
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.597 0.720 3 186853334 intron variant G/C;T snv 0.020 1.000 2 2014 2015
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1 2013 2013
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2016 2016
Familial multiple trichoepitheliomata
CUI: C1275122
Disease: Familial multiple trichoepitheliomata
32 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2008 2008
Generalized obesity
CUI: C0342942
Disease: Generalized obesity
4 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2013 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.597 0.720 3 186853334 intron variant G/C;T snv 0.050 0.800 5 2011 2019
Hypoadiponectinemia
CUI: C2675519
Disease: Hypoadiponectinemia
17 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2013 2013
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.597 0.720 3 186853334 intron variant G/C;T snv 0.030 3 2006 2015