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 0.597 0.720 3 186853334 intron variant G/C;T snv 0.100 0.923 13 2009 2019
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
Obesity
CUI: C0028754
Disease: Obesity
1111 0.597 0.720 3 186853334 intron variant G/C;T snv 0.060 1.000 6 2009 2019
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
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.597 0.720 3 186853334 intron variant G/C;T snv 0.050 0.800 5 2013 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.597 0.720 3 186853334 intron variant G/C;T snv 0.050 0.800 5 2013 2015
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
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.597 0.720 3 186853334 intron variant G/C;T snv 0.040 1.000 4 2011 2018
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.597 0.720 3 186853334 intron variant G/C;T snv 0.040 1.000 4 2015 2019
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
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
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
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.597 0.720 3 186853334 intron variant G/C;T snv 0.030 1.000 3 2008 2013
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.597 0.720 3 186853334 intron variant G/C;T snv 0.030 0.667 3 2006 2018
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.597 0.720 3 186853334 intron variant G/C;T snv 0.030 1.000 3 2013 2018
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
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.597 0.720 3 186853334 intron variant G/C;T snv 0.020 1.000 2 2011 2013
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.597 0.720 3 186853334 intron variant G/C;T snv 0.020 1.000 2 2011 2012
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.597 0.720 3 186853334 intron variant G/C;T snv 0.020 1.000 2 2019 2019
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.597 0.720 3 186853334 intron variant G/C;T snv 0.020 1.000 2 2011 2013
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
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