Source: UNIPROT

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: rs121913500
rs121913500
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06
CUI: C0017638
Disease: Glioma
Glioma
0.800 1.000 0 2009 2019
dbSNP: rs121913499
rs121913499
0.605 0.520 2 208248389 missense variant G/A;C;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.720 1.000 0 2011 2012
dbSNP: rs104894156
rs104894156
1.000 0.040 10 122582793 missense variant G/T snv
CUI: C0017638
Disease: Glioma
Glioma
0.700 0
dbSNP: rs1064794096
rs1064794096
1.000 0.040 10 87864514 missense variant A/C;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.700 0
dbSNP: rs1554893792
rs1554893792
1.000 0.040 10 87894052 missense variant G/A snv
CUI: C0017638
Disease: Glioma
Glioma
0.700 0
dbSNP: rs63751110
rs63751110
0.925 0.160 2 47410322 missense variant T/C;G snv
CUI: C0017638
Disease: Glioma
Glioma
0.700 0
dbSNP: rs786202398
rs786202398
0.925 0.080 10 87925518 stop gained T/A;G snv
CUI: C0017638
Disease: Glioma
Glioma
0.700 0