Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs11670188
BTBD2
0.925 0.040 19 2014038 non coding transcript exon variant A/G snv 0.16 2
rs118101777
IDH2
0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs11860248
RBBP6
0.882 0.040 16 24566445 intron variant T/G snv 0.27 5
rs11979158
EGFR
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 5
rs1205454520
KLLN ; PTEN
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06 10
rs1210653597
CDKN2A
0.925 0.120 9 21968756 missense variant T/C snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909218
PTEN
0.672 0.360 10 87933145 missense variant G/A snv 25
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs12230172
LOC105369844
0.882 0.040 12 75848895 intron variant A/G snv 0.48 4
rs1249080185
EPHB2
0.882 0.080 1 22784698 missense variant G/A snv 3
rs1259560536
ADAM33
1.000 0.040 20 3671756 missense variant T/C snv 7.0E-06 1
rs12645561
NEIL3
0.882 0.120 4 177339718 intron variant C/A;T snv 3
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs12752552
RAVER2
0.882 0.040 1 64763616 intron variant T/C snv 0.13 4