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: 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
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0036572
Disease: Seizures
Seizures
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: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis
0.010 1.000 1 2004 2004
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
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
Secondary malignant neoplasm of lymph node
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
Necrotizing enterocolitis in fetus OR newborn
0.010 < 0.001 1 2016 2016
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0011303
Disease: Demyelinating Diseases
Demyelinating Diseases
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: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.010 1.000 1 2016 2016
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
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: C0948008
Disease: Ischemic stroke
Ischemic stroke
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: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
Laryngeal Squamous Cell Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
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: C0010346
Disease: Crohn Disease
Crohn Disease
0.010 1.000 1 2017 2017