Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10146204 1.000 0.120 14 64352051 non coding transcript exon variant G/A snv 0.45 2
rs1018379423
EPHB2
1 22907986 missense variant G/T snv 4.0E-06 2.1E-05 4
rs1052559
KLC3 ; ERCC2
1.000 0.040 19 45351661 stop gained T/A;G snv 2
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs112295309
SCRIB ; MIR937
1.000 0.080 8 143813896 missense variant T/C;G snv 6.1E-04 3
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1174029586
CANX
5 179705693 missense variant G/C snv 8.2E-06 1
rs1192694481
MMP13
0.882 0.080 11 102955629 missense variant C/T snv 4.0E-06 4
rs12072037
MFSD2A
0.882 0.080 1 39954534 upstream gene variant C/A snv 6.1E-02 4
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1238968510
MMP2
0.882 0.080 16 55479556 missense variant A/G;T snv 4.1E-06 2.1E-05 4
rs1242640031
CRK
17 1456106 missense variant G/C snv 1
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 5
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1444669684
CDKN2B-AS1 ; CDKN2A
0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1458974438
STK11
0.807 0.080 19 1206957 missense variant G/A snv 9
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19