Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10131032
AKAP6
1.000 0.040 14 32780875 intron variant G/A snv 9.3E-02 2
rs10494090
SLC25A24
1.000 0.040 1 108150714 intron variant A/C;G;T snv 2
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs10852606
HEATR3
0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs10924303
LOC105373265 ; KIF26B
1.000 0.040 1 245683732 intron variant C/T snv 0.15 2
rs10924690
SMYD3
1.000 0.040 1 246320481 intron variant G/A snv 0.20 2
rs11163687
LOC107985037
1.000 0.040 1 83199436 intergenic variant A/G snv 9.6E-02 2
rs11166389
SLC35A3 ; RNU6-1318P
1.000 0.040 1 100000723 non coding transcript exon variant G/A snv 0.15 2
rs111696067
GOLGA3
1.000 0.040 12 132799954 intron variant T/C snv 5.3E-04 2
rs11233250
MIR4300HG
0.882 0.040 11 82685972 intron variant C/T snv 0.11 4
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11583706
LOC105373220
1.000 0.040 1 238358337 intron variant G/T snv 0.17 2
rs11598018
STN1
1.000 0.040 10 103901557 intron variant C/A;T snv 2
rs11599775
VTI1A
1.000 0.040 10 112699938 intron variant G/A snv 0.27 2
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs11706832
LRIG1
1.000 0.040 3 66452557 intron variant A/C;G snv 2
rs11979158
EGFR
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 5
rs12021720
DBT
0.925 0.160 1 100206504 missense variant T/A;C snv 0.92 3
rs12076373
AKT3
1.000 0.040 1 243688645 intron variant G/C snv 0.20 2
rs12088062 1.000 0.040 1 244811284 intergenic variant C/T snv 0.20 2
rs12125049
LINC02778 ; LOC105378761
1.000 0.040 1 60202030 intergenic variant C/T snv 0.12 2
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs12230172
LOC105369844
0.882 0.040 12 75848895 intron variant A/G snv 0.48 4