rs1034749666, OLIG2

N. diseases: 9
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.
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.776 0.160 21 33027257 missense variant G/A snv 0.030 0.667 3 2014 2017
Adult Oligodendroglioma
CUI: C0279070
Disease: Adult Oligodendroglioma
19 0.776 0.160 21 33027257 missense variant G/A snv 0.010 1.000 1 2013 2013
ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED
CUI: C1845055
Disease: ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED
32 0.776 0.160 21 33027257 missense variant G/A snv 0.010 1.000 1 2017 2017
Childhood Oligodendroglioma
CUI: C0280475
Disease: Childhood Oligodendroglioma
19 0.776 0.160 21 33027257 missense variant G/A snv 0.010 1.000 1 2013 2013
Ganglioneuroma
CUI: C0017075
Disease: Ganglioneuroma
2 0.776 0.160 21 33027257 missense variant G/A snv 0.010 1.000 1 2013 2013
Glioma
CUI: C0017638
Disease: Glioma
353 0.776 0.160 21 33027257 missense variant G/A snv 0.010 1.000 1 2016 2016
Hurthle Cell Tumor
CUI: C0949541
Disease: Hurthle Cell Tumor
9 0.776 0.160 21 33027257 missense variant G/A snv 0.010 1.000 1 2013 2013
oligodendroglioma
CUI: C0028945
Disease: oligodendroglioma
21 0.776 0.160 21 33027257 missense variant G/A snv 0.010 1.000 1 2013 2013
Well Differentiated Oligodendroglioma
CUI: C0751396
Disease: Well Differentiated Oligodendroglioma
22 0.776 0.160 21 33027257 missense variant G/A snv 0.010 1.000 1 2013 2013