Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227983
EGFR
0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs752021744
PIK3CB
0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs372043866
ERBB2
0.732 0.240 17 39727965 missense variant G/A;C;T snv 3.2E-05; 2.4E-05; 1.2E-05 18
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs2107425
MRPL23 ; H19
0.732 0.280 11 1999845 intron variant C/T snv 16
rs1800372
TP53
0.752 0.240 17 7674892 synonymous variant T/A;C snv 1.3E-02 15
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs1060503115
PMS2
0.763 0.400 7 5978664 missense variant T/A;G snv 13
rs1289543302
ABCB1
0.763 0.440 7 87536472 missense variant C/T snv 12
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 11
rs746284240
MDM2
0.763 0.240 12 68809243 missense variant A/G snv 11
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 10
rs28929495
EGFR
0.807 0.120 7 55174014 missense variant G/A;C;T snv 9
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