Source: BEFREE

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: rs11979158
rs11979158
EGFR
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20
CUI: C0017638
Disease: Glioma
Glioma 		0.850 1.000 5 2011 2018
dbSNP: rs1801275
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0017638
Disease: Glioma
Glioma 		0.050 1.000 5 2011 2016
dbSNP: rs12917
rs12917
MGMT ; LOC105378560
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0017638
Disease: Glioma
Glioma 		0.040 1.000 4 2009 2018
dbSNP: rs1695
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36
CUI: C0017638
Disease: Glioma
Glioma 		0.040 0.500 4 2003 2014
dbSNP: rs1799793
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29
CUI: C0017638
Disease: Glioma
Glioma 		0.040 0.500 4 2012 2017
dbSNP: rs2853676
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv
CUI: C0017638
Disease: Glioma
Glioma 		0.840 1.000 4 2009 2017
dbSNP: rs730437
rs730437
EGFR
0.925 0.120 7 55147325 intron variant A/C snv 0.51
CUI: C0017638
Disease: Glioma
Glioma 		0.040 0.750 4 2012 2017
dbSNP: rs1217691063
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C0017638
Disease: Glioma
Glioma 		0.030 0.667 3 2013 2018
dbSNP: rs1346786
rs1346786
EFEMP1
1.000 0.040 2 55881198 intron variant C/T snv 0.36
CUI: C0017638
Disease: Glioma
Glioma 		0.030 1.000 3 2015 2017
dbSNP: rs1346787
rs1346787
EFEMP1 ; LOC112268416
0.882 0.040 2 55865477 downstream gene variant C/A;G;T snv
CUI: C0017638
Disease: Glioma
Glioma 		0.030 1.000 3 2015 2017
dbSNP: rs1468727
rs1468727
EGFR
0.925 0.120 7 55162412 intron variant C/T snv 0.21
CUI: C0017638
Disease: Glioma
Glioma 		0.030 1.000 3 2012 2015
dbSNP: rs1805377
rs1805377
XRCC4
0.689 0.480 5 83353124 splice acceptor variant G/A snv 0.23 0.25
CUI: C0017638
Disease: Glioma
Glioma 		0.030 0.667 3 2013 2017
dbSNP: rs2010963
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0017638
Disease: Glioma
Glioma 		0.030 1.000 3 2011 2018
dbSNP: rs2276466
rs2276466
ERCC4
0.732 0.320 16 13949318 3 prime UTR variant C/A;G snv
CUI: C0017638
Disease: Glioma
Glioma 		0.030 1.000 3 2013 2014
dbSNP: rs3791679
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20
CUI: C0017638
Disease: Glioma
Glioma 		0.030 1.000 3 2015 2016
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0017638
Disease: Glioma
Glioma 		0.030 1.000 3 2012 2014
dbSNP: rs10131
rs10131
LIG4
1.000 0.040 13 108207498 3 prime UTR variant C/T snv 0.12
CUI: C0017638
Disease: Glioma
Glioma 		0.020 1.000 2 2015 2016
dbSNP: rs1045485
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02
CUI: C0017638
Disease: Glioma
Glioma 		0.020 1.000 2 2008 2016
dbSNP: rs1059394
rs1059394
TYMS ; ENOSF1
0.925 0.080 18 672792 3 prime UTR variant C/T snv 0.40
CUI: C0017638
Disease: Glioma
Glioma 		0.020 1.000 2 2019 2019
dbSNP: rs11196067
rs11196067
VTI1A
0.752 0.160 10 112709306 intron variant A/T snv 0.32
CUI: C0017638
Disease: Glioma
Glioma 		0.020 1.000 2 2017 2018
dbSNP: rs11614913
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0017638
Disease: Glioma
Glioma 		0.020 1.000 2 2010 2017
dbSNP: rs11615
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55
CUI: C0017638
Disease: Glioma
Glioma 		0.020 0.500 2 2012 2017
dbSNP: rs121913499
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv
CUI: C0017638
Disease: Glioma
Glioma 		0.720 1.000 2 2011 2012
dbSNP: rs17655
rs17655
ERCC5 ; BIVM-ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30
CUI: C0017638
Disease: Glioma
Glioma 		0.020 1.000 2 2017 2017
dbSNP: rs1800925
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv
CUI: C0017638
Disease: Glioma
Glioma 		0.020 1.000 2 2013 2015