rs4880, SOD2

N. diseases: 131
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Malignant neoplasm of skin
CUI: C0007114
Disease: Malignant neoplasm of skin
38 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2007 2007
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2012 2012
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2017 2017
B-Cell Lymphomas
CUI: C0079731
Disease: B-Cell Lymphomas
42 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2006 2006
Dyskinetic syndrome
CUI: C0013384
Disease: Dyskinetic syndrome
42 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2019 2019
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2016 2016
Malignant neoplasm of larynx
CUI: C0007107
Disease: Malignant neoplasm of larynx
50 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2013 2013
Primary angle-closure glaucoma
CUI: C0017606
Disease: Primary angle-closure glaucoma
55 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2015 2015
Angle Closure Glaucoma
CUI: C0017605
Disease: Angle Closure Glaucoma
56 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2015 2015
Hereditary hemochromatosis
CUI: C0392514
Disease: Hereditary hemochromatosis
56 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2004 2004
Migraine with Aura
CUI: C0154723
Disease: Migraine with Aura
56 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2015 2015
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2010 2010
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2014 2014
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2013 2013
Sporadic Parkinson disease
CUI: C4511452
Disease: Sporadic Parkinson disease
65 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2014 2014
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2006 2006
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2006 2006
Drug-induced tardive dyskinesia
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
67 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.020 0.500 2 2008 2010
Tardive Dyskinesia
CUI: C0686347
Disease: Tardive Dyskinesia
67 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.020 0.500 2 2008 2010
Polypoidal choroidal vasculopathy
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
67 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1 2009 2009
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2012 2012
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2012 2012
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2014 2014
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2006 2006
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.010 1.000 1 2013 2013