Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1346786
rs1346786
1.000 0.040 2 55881198 intron variant C/T snv 0.36
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.030 1.000 3 2015 2017
dbSNP: rs1346787
rs1346787
0.882 0.040 2 55865477 downstream gene variant C/A;G;T snv
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.030 1.000 3 2015 2017
dbSNP: rs3791679
rs3791679
0.925 0.120 2 55869757 intron variant A/G snv 0.20
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.030 1.000 3 2015 2016
dbSNP: rs1344733
rs1344733
1.000 0.040 2 55900892 intron variant T/C snv 0.41
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs3791675
rs3791675
1.000 0.040 2 55884174 intron variant C/T snv 0.20
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs727878
rs727878
1.000 0.040 2 55892522 intron variant C/T snv 0.40
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.010 1.000 1 2015 2015