Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
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
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1444669684
CDKN2B-AS1 ; CDKN2A
0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs3743073
CHRNA3
0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1458974438
STK11
0.807 0.080 19 1206957 missense variant G/A snv 9
rs588765
CHRNA5
0.827 0.200 15 78573083 intron variant T/A;C snv 6
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 5
rs12072037
MFSD2A
0.882 0.080 1 39954534 upstream gene variant C/A snv 6.1E-02 4
rs6808523
SATB1 ; TBC1D5
0.882 0.080 3 18430796 intron variant A/G snv 8.0E-02 4
rs10146204 1.000 0.120 14 64352051 non coding transcript exon variant G/A snv 0.45 2
rs1052559
KLC3 ; ERCC2
1.000 0.040 19 45351661 stop gained T/A;G snv 2
rs1242640031
CRK
17 1456106 missense variant G/C snv 1
rs8021944
ESR2 ; SYNE2
14 64212580 intron variant T/G snv 5.6E-02 1
rs1018379423
EPHB2
1 22907986 missense variant G/T snv 4.0E-06 2.1E-05 4
rs759404153
EPHB2
1.000 0.040 1 22910452 missense variant T/A;G snv 2.8E-05; 4.0E-06 2
rs775514340
CILK1
0.882 0.080 6 53041202 missense variant T/A;C snv 4.0E-06 5
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12
rs1192694481
MMP13
0.882 0.080 11 102955629 missense variant C/T snv 4.0E-06 4
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134