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: rs1005230
rs1005230
0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2018 2018
dbSNP: rs10165970
rs10165970
0.708 0.320 2 100840527 intron variant G/A snv 0.16
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2017 2017
dbSNP: rs1034749666
rs1034749666
0.776 0.160 21 33027257 missense variant G/A snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2016 2016
dbSNP: rs1044129
rs1044129
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2019 2019
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0017638
Disease: Glioma
Glioma
0.010 < 0.001 1 2005 2005
dbSNP: rs1048771
rs1048771
1.000 0.040 1 46278228 synonymous variant C/A;T snv 4.0E-06; 0.15
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2016 2016
dbSNP: rs104894104
rs104894104
0.790 0.160 9 21971019 missense variant G/A;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 1997 1997
dbSNP: rs1049353
rs1049353
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2010 2010
dbSNP: rs10506868
rs10506868
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2018 2018
dbSNP: rs10519097
rs10519097
0.708 0.320 15 60997989 intron variant C/T snv 0.13
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2017 2017
dbSNP: rs1052555
rs1052555
0.882 0.040 19 45352266 synonymous variant G/A snv 0.28 0.26
CUI: C0017638
Disease: Glioma
Glioma
0.010 < 0.001 1 2014 2014
dbSNP: rs1052576
rs1052576
0.807 0.200 1 15506048 missense variant T/A;C snv 0.53
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2017 2017
dbSNP: rs1053667
rs1053667
0.925 0.120 14 45073835 3 prime UTR variant T/C snv 0.11
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2019 2019
dbSNP: rs1057519902
rs1057519902
0.742 0.160 1 226064451 missense variant G/C snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2019 2019
dbSNP: rs1058319
rs1058319
1.000 0.040 20 63743036 3 prime UTR variant C/A;T snv 0.21
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2012 2012
dbSNP: rs1059513
rs1059513
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2011 2011
dbSNP: rs10764901
rs10764901
1.000 0.040 10 129716598 intron variant A/G snv 0.62
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2018 2018
dbSNP: rs11079041
rs11079041
0.882 0.040 17 42262061 intron variant T/A;C snv 0.36
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2014 2014
dbSNP: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2018 2018
dbSNP: rs1131239
rs1131239
1.000 0.040 4 121696590 5 prime UTR variant G/A;C;T snv 0.12 0.17
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2019 2019
dbSNP: rs11337
rs11337
0.925 0.120 8 41510767 3 prime UTR variant T/G snv 0.93
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2019 2019
dbSNP: rs1138272
rs1138272
0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2013 2013
dbSNP: rs11506105
rs11506105
0.851 0.160 7 55152484 intron variant A/G snv 0.59
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2017 2017
dbSNP: rs115303435
rs115303435
1.000 0.040 20 63694806 missense variant G/A snv 3.2E-03 1.1E-03
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2018 2018
dbSNP: rs11554137
rs11554137
0.742 0.040 2 208248468 synonymous variant G/A snv 5.1E-02 6.8E-02
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2018 2018