Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs281432
rs281432
0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 < 0.001 1 2016 2016
dbSNP: rs281432
rs281432
0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0940937
Disease: precancerous lesions
precancerous lesions
0.010 1.000 1 2016 2016
dbSNP: rs281432
rs281432
0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0002962
Disease: Angina Pectoris
Angina Pectoris
0.010 1.000 1 2015 2015
dbSNP: rs281432
rs281432
0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 1.000 1 2015 2015
dbSNP: rs281432
rs281432
0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0677898
Disease: invasive cancer
invasive cancer
0.010 1.000 1 2016 2016
dbSNP: rs281432
rs281432
0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2015 2015
dbSNP: rs281432
rs281432
0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 1.000 1 2006 2006
dbSNP: rs281432
rs281432
0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs281432
rs281432
0.851 0.280 19 10279982 intron variant C/G snv 0.52
Diabetes Mellitus, Insulin-Dependent
0.010 1.000 1 2006 2006
dbSNP: rs281432
rs281432
0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2016 2016
dbSNP: rs281432
rs281432
0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2015 2015
dbSNP: rs281432
rs281432
0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 < 0.001 1 2016 2016
dbSNP: rs5496
rs5496
1.000 0.080 19 10284771 intron variant G/A snv 7.8E-03 3.3E-02
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
0.010 1.000 1 2013 2013
dbSNP: rs5498
rs5498
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.090 1.000 9 2009 2019
dbSNP: rs5498
rs5498
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
Diabetes Mellitus, Non-Insulin-Dependent
0.090 0.778 9 2005 2019
dbSNP: rs5498
rs5498
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.060 1.000 6 2009 2018
dbSNP: rs5498
rs5498
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.060 0.833 6 2004 2018
dbSNP: rs5498
rs5498
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
0.060 0.500 6 2006 2018
dbSNP: rs5498
rs5498
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.060 1.000 6 2003 2015
dbSNP: rs5498
rs5498
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.050 1.000 5 2003 2019
dbSNP: rs5498
rs5498
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.050 0.600 5 2003 2016
dbSNP: rs5498
rs5498
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.050 1.000 5 2006 2018
dbSNP: rs5498
rs5498
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
Diabetes Mellitus, Insulin-Dependent
0.050 0.600 5 2000 2019
dbSNP: rs1799969
rs1799969
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.040 0.500 4 2003 2016
dbSNP: rs5498
rs5498
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.040 0.750 4 2006 2018