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: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.020 1.000 2 2006 2012
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.020 1.000 2 2006 2009
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.020 1.000 2 2008 2009
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior 		0.020 1.000 2 2006 2012
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2014 2014
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		0.010 1.000 1 2006 2006
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		0.010 1.000 1 2011 2011
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0497327
Disease: Dementia
Dementia 		0.010 1.000 1 2017 2017
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome 		0.010 1.000 1 2017 2017
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		0.010 < 0.001 1 2015 2015
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		0.010 1.000 1 2017 2017
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.010 1.000 1 2016 2016
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		0.010 1.000 1 2014 2014
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0006625
Disease: Cachexia
Cachexia 		0.010 1.000 1 2017 2017
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2011 2011
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2011 2011
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0085077
Disease: Sweet Syndrome
Sweet Syndrome 		0.010 1.000 1 2017 2017
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0039101
Disease: synovial sarcoma
synovial sarcoma 		0.010 1.000 1 2017 2017
dbSNP: rs4291
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy 		0.010 1.000 1 2017 2017