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: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.030 0.667 3 2005 2010
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary 		0.030 0.667 3 2005 2010
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial 		0.030 0.667 3 2005 2010
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.020 1.000 2 2005 2015
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.020 0.500 2 2005 2006
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.020 0.500 2 2009 2015
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0010072
Disease: Coronary Thrombosis
Coronary Thrombosis 		0.020 1.000 2 2004 2014
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.020 1.000 2 2011 2014
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.020 1.000 2 2015 2017
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.020 1.000 2 2005 2016
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.020 0.500 2 1997 2018
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.020 0.500 2 2005 2006
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.020 1.000 2 2005 2015
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0577698
Disease: Exercise-induced angina
Exercise-induced angina 		0.010 1.000 1 2007 2007
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		0.010 1.000 1 2017 2017
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 < 0.001 1 2009 2009
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2011 2011
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		0.010 1.000 1 2014 2014
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2015 2015
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2015 2015
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.010 < 0.001 1 2015 2015
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.010 1.000 1 2017 2017
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2011 2011
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2016 2016
dbSNP: rs5918
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior 		0.010 1.000 1 2017 2017