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: 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: 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: 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: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.710 1.000 1 2009 2018
dbSNP: rs11571378
rs11571378
0.925 0.080 12 950115 intron variant A/C;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2014 2014
dbSNP: rs11706832
rs11706832
1.000 0.040 3 66452557 intron variant A/C;G snv
CUI: C0017638
Disease: Glioma
Glioma
0.710 1.000 1 2017 2018
dbSNP: rs1197458016
rs1197458016
1.000 0.040 9 15466782 missense variant T/C snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2016 2016
dbSNP: rs1214285376
rs1214285376
0.776 0.200 19 43543490 missense variant G/T snv 4.0E-06
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2014 2014
dbSNP: rs121912660
rs121912660
0.683 0.240 17 7673781 missense variant C/A;G;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2012 2012
dbSNP: rs12615793
rs12615793
0.851 0.280 2 54248777 intron variant G/A;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2017 2017
dbSNP: rs1273593548
rs1273593548
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2017 2017
dbSNP: rs1345354331
rs1345354331
1.000 0.040 3 49358221 missense variant A/C;T snv 6.8E-06; 6.8E-06
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2012 2012
dbSNP: rs1353702185
rs1353702185
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2012 2012
dbSNP: rs1373481065
rs1373481065
0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2017 2017
dbSNP: rs1385943435
rs1385943435
0.851 0.040 9 37002662 missense variant C/A;G;T snv 4.1E-06; 4.1E-06
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2012 2012
dbSNP: rs1431316232
rs1431316232
1.000 0.040 9 22006021 missense variant A/G snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 1997 1997
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2017 2017
dbSNP: rs148611340
rs148611340
0.790 0.120 19 43543621 missense variant G/A;C snv 4.0E-06; 1.2E-05
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2014 2014
dbSNP: rs1553260624
rs1553260624
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2019 2019
dbSNP: rs1625895
rs1625895
0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2007 2007
dbSNP: rs1642785
rs1642785
0.807 0.200 17 7676483 5 prime UTR variant G/A;C;T snv 1.2E-05; 0.67; 2.8E-05
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2011 2011