Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs147001633
DNMT3A
0.776 0.240 2 25234373 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.2E-04 15
rs863225281
ALK
0.776 0.200 2 29220829 missense variant G/C;T snv 12
rs3827760
RANBP2 ; EDAR
0.752 0.160 2 108897145 missense variant A/G snv 0.15 5.9E-02 11
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 10
rs1057519781
ALK
0.807 0.160 2 29209816 missense variant C/G snv 9
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1057519920
NFE2L2
0.790 0.160 2 177234232 missense variant C/A;G;T snv 7
rs1057519922
NFE2L2
0.790 0.200 2 177234082 missense variant C/G;T snv 7
rs377577594
DNMT3A
0.827 0.240 2 25234374 missense variant G/A;C;T snv 1.2E-04; 8.0E-06 7
rs1057519923
NFE2L2
0.807 0.200 2 177234081 missense variant T/A snv 6
rs1057519924
NFE2L2
0.807 0.200 2 177234080 missense variant C/A snv 6
rs772399455
MYCNOS ; MYCN
0.851 0.080 2 15942096 missense variant G/A;C snv 4.0E-06 6
rs4953354
EPAS1
0.827 0.120 2 46348249 intron variant A/G snv 0.22 5
rs759435862
KIDINS220
0.925 0.080 2 8776852 missense variant C/A;T snv 2.0E-05 5
rs1057519785
ALK
1.000 0.040 2 29222404 missense variant A/C snv 2
rs1057519963
SOS1
0.925 0.080 2 39054637 missense variant T/A snv 2
rs79294676
LINC01829 ; LINC01828
0.925 0.080 2 67277529 intron variant G/A snv 6.4E-03 2
rs1057519782
ALK
1.000 0.040 2 29220734 missense variant G/T snv 1
rs114928225 1.000 0.040 2 118692164 intergenic variant T/A snv 1.0E-02 1
rs148944993
LINC01891
1.000 0.040 2 234452501 intron variant G/A snv 2.0E-03 1
rs17038564
ACTR2
1.000 0.040 2 65268924 3 prime UTR variant A/G snv 5.3E-02 1
rs191524990
C1D
1.000 0.040 2 68069083 intron variant A/T snv 7.6E-03 1
rs59396197 1.000 0.040 2 139675756 intergenic variant G/A snv 9.1E-02 1