rs5918, ITGB3

N. diseases: 26
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.
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.030 0.667 3 2005 2010
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.030 0.667 3 2005 2010
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.030 0.667 3 2005 2010
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.020 0.500 2 2005 2006
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.020 1.000 2 2005 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.020 1.000 2 2011 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.020 0.500 2 2009 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.020 1.000 2 2015 2017
Coronary Thrombosis
CUI: C0010072
Disease: Coronary Thrombosis
2 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.020 1.000 2 2004 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.020 0.500 2 2005 2006
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.020 1.000 2 2005 2015
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.020 0.500 2 1997 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.020 1.000 2 2005 2015
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.010 1.000 1 2014 2014
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.010 1.000 1 2011 2011
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.010 1.000 1 2011 2011
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.010 1.000 1 2017 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.010 1.000 1 2015 2015
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.010 1.000 1 2015 2015
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.010 1.000 1 2017 2017
Exercise-induced angina
CUI: C0577698
Disease: Exercise-induced angina
5 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.010 1.000 1 2007 2007
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.010 1.000 1 2005 2005
Hyperactive behavior
CUI: C0424295
Disease: Hyperactive behavior
112 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.010 1.000 1 2017 2017
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.010 1.000 1 2016 2016
Malignant neoplasm of colon and/or rectum
502 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.010 1 2009 2009