Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397517108
EGFR ; EGFR-AS1
0.790 0.120 7 55181312 missense variant GC/TT mnv 9
rs754332870
TP53
0.790 0.240 17 7676240 missense variant C/G snv 4.0E-06 9
rs4645978
CASP9 ; DNAJC16
0.827 0.120 1 15525539 intron variant C/A;T snv 8
rs10810657 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 7
rs59912467
STK11
0.790 0.120 19 1223126 missense variant C/G;T snv 5.2E-03; 4.1E-06 7
rs1057520018
STK11
0.807 0.080 19 1223124 missense variant T/C snv 6
rs12108497
PRIMPOL ; CASP3
0.851 0.080 4 184650403 intron variant C/G;T snv 6
rs1389500636
EGFR
0.827 0.080 7 55156796 missense variant G/A snv 6
rs1454328441
MUC1
0.827 0.200 1 155192002 missense variant G/A;T snv 4.6E-06; 9.1E-06 6
rs35407
SLC45A2
0.807 0.080 5 33946466 3 prime UTR variant A/C;G snv 6
rs5491
ICAM1
0.827 0.160 19 10274864 missense variant A/G;T snv 4.0E-06; 2.8E-02 6
rs7208422
TMC8
0.807 0.120 17 78134494 missense variant A/C;T snv 4.0E-06; 0.51 6
rs2273953
TP73
0.851 0.120 1 3682336 5 prime UTR variant G/A;T snv 0.20; 3.3E-04 5
rs2299939
PTEN
0.827 0.080 10 87897393 intron variant C/A;T snv 5
rs587783064
TP53
0.851 0.120 17 7669626 missense variant C/A;T snv 5
rs1057520039
STK11
0.882 0.200 19 1207169 stop gained C/G;T snv 4
rs58330629
KRT14
0.851 0.120 17 41586461 missense variant C/A;G;T snv 4
rs765660823
DDR2
0.882 0.200 1 162778720 missense variant A/C snv 1.9E-04 4
rs868438023
KNSTRN
0.882 0.080 15 40382906 missense variant C/T snv 4
rs1770474
TNKS2
0.925 0.080 10 91833770 intron variant G/A;T snv 3
rs267598140
DDR2
0.925 0.080 1 162778600 missense variant T/A;G snv 3
rs471692
TOP2A
0.925 0.080 17 40400518 intron variant T/A;C snv 0.79 3
rs74664507 1.000 0.040 9 16913838 upstream gene variant T/A snv 3
rs804270
NEIL2
0.882 0.080 8 11770112 5 prime UTR variant G/C;T snv 3
rs121913082
FAS
1.000 0.040 10 89014205 missense variant A/G snv 2