rs699473, SOD3

N. diseases: 5
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.
Adult Meningioma
CUI: C0278877
Disease: Adult Meningioma
30 0.827 0.160 4 24795181 intron variant C/T snv 0.54 0.010 1.000 1 2008 2008
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.827 0.160 4 24795181 intron variant C/T snv 0.54 0.010 1.000 1 2008 2008
Glioma
CUI: C0017638
Disease: Glioma
353 0.827 0.160 4 24795181 intron variant C/T snv 0.54 0.010 1.000 1 2008 2008
Meningioma
CUI: C0025286
Disease: Meningioma
43 0.827 0.160 4 24795181 intron variant C/T snv 0.54 0.010 1.000 1 2008 2008
Meningioma, benign, no ICD-O subtype
CUI: C1762616
Disease: Meningioma, benign, no ICD-O subtype
30 0.827 0.160 4 24795181 intron variant C/T snv 0.54 0.010 1.000 1 2008 2008