rs2230806, ABCA1

N. diseases: 24
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.100 0.917 12 2003 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.100 1.000 11 2003 2019
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.090 0.889 9 2006 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.090 1.000 9 2003 2019
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.040 0.750 4 2003 2018
Obesity
CUI: C0028754
Disease: Obesity
1111 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.040 1.000 4 2007 2016
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.030 1.000 3 2003 2014
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.030 0.667 3 2015 2018
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.020 1.000 2 2006 2007
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.020 1.000 2 2014 2017
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1.000 1 2010 2010
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1.000 1 2006 2006
Familial hypercholesterolemia - heterozygous
34 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1.000 1 2004 2004
Heart Diseases
CUI: C0018799
Disease: Heart Diseases
45 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1.000 1 2014 2014
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1.000 1 2003 2003
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1.000 1 2003 2003
Infarction, Lacunar
CUI: C0333559
Disease: Infarction, Lacunar
18 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1 2018 2018
Intracranial Aneurysm
CUI: C0007766
Disease: Intracranial Aneurysm
150 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1.000 1 2015 2015
Mild cognitive disorder
CUI: C1270972
Disease: Mild cognitive disorder
96 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1.000 1 2017 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1.000 1 2004 2004
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1.000 1 2017 2017
Premature coronary artery atherosclerosis
43 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1.000 1 2015 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 0.010 1.000 1 2015 2015