Source: ALL

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: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.020 1.000 2 2010 2012
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia
0.020 0.500 2 2008 2010
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.020 1.000 2 2010 2010
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0004096
Disease: Asthma
Asthma
0.020 1.000 2 2004 2006
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia
0.020 0.500 2 2008 2010
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.020 1.000 2 2008 2011
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C1623038
Disease: Cirrhosis
Cirrhosis
0.020 1.000 2 2011 2012
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 1.000 2 2011 2012
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.020 1.000 2 2010 2012
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.020 1.000 2 2017 2019
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.020 1.000 2 2007 2009
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.020 1.000 2 2010 2010
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases
0.010 1.000 1 2017 2017
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle
0.010 < 0.001 1 2015 2015
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0027859
Disease: Acoustic Neuroma
Acoustic Neuroma
0.010 1.000 1 2008 2008
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C3146264
Disease: Stage IV Prostate Cancer AJCC v7
Stage IV Prostate Cancer AJCC v7
0.010 1.000 1 2015 2015
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0013384
Disease: Dyskinetic syndrome
Dyskinetic syndrome
0.010 1.000 1 2019 2019
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0750151
Disease: Vaso-Occlusive Crisis
Vaso-Occlusive Crisis
0.010 1.000 1 2018 2018
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
0.010 1.000 1 2011 2011
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 1.000 1 2009 2009
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma
0.010 1.000 1 2006 2006
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.010 1.000 1 2009 2009
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0003949
Disease: Asbestosis
Asbestosis
0.010 1.000 1 2008 2008
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0025281
Disease: Meniere Disease
Meniere Disease
0.010 1.000 1 2012 2012
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0860207
Disease: Drug-Induced Liver Disease
Drug-Induced Liver Disease
0.010 1.000 1 2010 2010