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: rs1217691063
rs1217691063
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: 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: rs1695
rs1695
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: rs1800562
rs1800562
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2011 2011
dbSNP: rs2910164
rs2910164
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2011 2011
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2017 2017
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: rs2010963
rs2010963
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: 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: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2007 2007
dbSNP: rs1801131
rs1801131
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2017 2017
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2017 2017
dbSNP: rs3212227
rs3212227
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2012 2012
dbSNP: rs662
rs662
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2015 2015
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: 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: 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: 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: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2016 2016
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2010 2010
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0017638
Disease: Glioma
Glioma
0.010 < 0.001 1 2016 2016
dbSNP: rs5743708
rs5743708
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2019 2019
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2015 2015