Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs25489
XRCC1
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 17
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 16
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs4295627
CCDC26
0.763 0.200 8 129673211 intron variant T/G snv 0.17 11
rs498872
PHLDB1
0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 10
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81 10
rs63749993
MSH2
0.882 0.200 2 47476424 missense variant T/G snv 8
rs35850753
TP53
0.807 0.080 17 7675353 5 prime UTR variant C/T snv 1.3E-02 8
rs4809324
RTEL1 ; RTEL1-TNFRSF6B
0.807 0.200 20 63686867 non coding transcript exon variant T/C snv 8.8E-02 7
rs634537
CDKN2B-AS1
0.851 0.080 9 22032153 intron variant T/G snv 0.28 6
rs2252586 0.882 0.040 7 54911231 intergenic variant C/T snv 0.27 5
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17 5