Source: ALL

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 49 2009 2019
dbSNP: rs6010620
rs6010620
0.701 0.360 20 63678486 intron variant A/C;G snv
CUI: C0017638
Disease: Glioma
Glioma
0.900 0.952 21 2009 2020
dbSNP: rs121913377
rs121913377
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv
CUI: C0017638
Disease: Glioma
Glioma
0.100 1.000 19 2011 2020
dbSNP: rs113488022
rs113488022
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C0017638
Disease: Glioma
Glioma
0.100 1.000 18 2011 2020
dbSNP: rs2736100
rs2736100
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52
CUI: C0017638
Disease: Glioma
Glioma
0.900 0.889 18 2009 2020
dbSNP: rs498872
rs498872
0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.900 0.941 17 2009 2020
dbSNP: rs4977756
rs4977756
0.683 0.440 9 22068653 intron variant G/A snv 0.64
CUI: C0017638
Disease: Glioma
Glioma
0.900 0.875 16 2009 2020
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0017638
Disease: Glioma
Glioma
0.100 0.933 15 2010 2017
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0017638
Disease: Glioma
Glioma
0.100 0.929 14 2010 2017
dbSNP: rs4295627
rs4295627
0.763 0.200 8 129673211 intron variant T/G snv 0.17
CUI: C0017638
Disease: Glioma
Glioma
0.900 1.000 12 2009 2020
dbSNP: rs13181
rs13181
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32
CUI: C0017638
Disease: Glioma
Glioma
0.100 1.000 11 2005 2017
dbSNP: rs25489
rs25489
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02
CUI: C0017638
Disease: Glioma
Glioma
0.090 0.889 9 2012 2017
dbSNP: rs55705857
rs55705857
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02
CUI: C0017638
Disease: Glioma
Glioma
0.760 1.000 9 2013 2019
dbSNP: rs1042522
rs1042522
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67
CUI: C0017638
Disease: Glioma
Glioma
0.080 0.625 8 2008 2018
dbSNP: rs1136410
rs1136410
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15
CUI: C0017638
Disease: Glioma
Glioma
0.080 1.000 8 2009 2019
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0017638
Disease: Glioma
Glioma
0.080 0.875 8 2012 2017
dbSNP: rs1131691014
rs1131691014
0.439 0.800 17 7676154 frameshift variant -/C ins
CUI: C0017638
Disease: Glioma
Glioma
0.070 0.571 7 2008 2018
dbSNP: rs3212986
rs3212986
0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06
CUI: C0017638
Disease: Glioma
Glioma
0.070 0.857 7 2014 2017
dbSNP: rs55819519
rs55819519
0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04
CUI: C0017638
Disease: Glioma
Glioma
0.070 1.000 7 2010 2019
dbSNP: rs878854066
rs878854066
0.439 0.800 17 7676153 missense variant GG/AC mnv
CUI: C0017638
Disease: Glioma
Glioma
0.070 0.571 7 2008 2018
dbSNP: rs11979158
rs11979158
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20
CUI: C0017638
Disease: Glioma
Glioma
0.850 1.000 6 2011 2018
dbSNP: rs1800067
rs1800067
0.716 0.320 16 13935176 missense variant G/A snv 5.6E-02 5.3E-02
CUI: C0017638
Disease: Glioma
Glioma
0.060 1.000 6 2013 2017
dbSNP: rs20541
rs20541
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77
CUI: C0017638
Disease: Glioma
Glioma
0.060 1.000 6 2010 2018
dbSNP: rs2252586
rs2252586
0.882 0.040 7 54911231 intergenic variant C/T snv 0.27
CUI: C0017638
Disease: Glioma
Glioma
0.860 0.833 6 2011 2017
dbSNP: rs2853676
rs2853676
0.667 0.560 5 1288432 intron variant T/A;C snv
CUI: C0017638
Disease: Glioma
Glioma
0.840 1.000 6 2009 2017