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: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.030 0.667 3 2008 2016
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0240912
Disease: Vertical Talus
Vertical Talus 		0.020 1.000 2 2014 2018
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.020 0.500 2 2018 2019
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		0.010 1.000 1 2009 2009
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2015 2015
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		0.010 1.000 1 2016 2016
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0039240
Disease: Supraventricular tachycardia
Supraventricular tachycardia 		0.010 1.000 1 2007 2007
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.010 1.000 1 2016 2016
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2005 2005
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2008 2008
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0025295
Disease: Meningitis, Pneumococcal
Meningitis, Pneumococcal 		0.010 1.000 1 2015 2015
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 < 0.001 1 2018 2018
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.010 1.000 1 2014 2014
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0002962
Disease: Angina Pectoris
Angina Pectoris 		0.010 1.000 1 2003 2003
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		0.010 1.000 1 2012 2012
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0002965
Disease: Angina, Unstable
Angina, Unstable 		0.010 1.000 1 2003 2003
dbSNP: rs3742264
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.010 1.000 1 2006 2006