Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs756090401
APC
1.000 0.080 5 112835036 missense variant A/G snv 8.0E-06 1.4E-05 1
rs1452020002
ERBB4
1.000 0.080 2 211947467 missense variant G/C;T snv 1
rs773197447
FGFR3
1.000 0.080 4 1807159 missense variant G/A;C snv 3.2E-05; 2.3E-05 1
rs1345316856
PBK ; ESCO2
1.000 0.080 8 27810979 missense variant A/C snv 4.0E-06 1
rs4872077
TNFRSF10A
1.000 0.080 8 23200675 intron variant T/A;C snv 0.29 1
rs876660572
APC
1.000 0.080 5 112815549 missense variant A/G snv 7.0E-06 2
rs758204762
ERBB2
0.925 0.080 17 39712330 missense variant G/A;C snv 4.0E-06; 1.6E-05 2
rs121913247
MET
0.882 0.200 7 116783359 missense variant T/C snv 3
rs397517096
EGFR
0.851 0.120 7 55174776 missense variant TT/CC mnv 4
rs1057519803
ERBB3
0.925 0.080 12 56088138 missense variant G/A snv 4
rs7553007 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 7
rs1057519742
GNA11
0.827 0.160 19 3118944 missense variant A/C;T snv 7
rs1057519909
MAP2K1
0.790 0.240 15 66435116 missense variant A/C snv 7
rs765433422
PTEN
0.807 0.160 10 87952250 stop gained G/A;T snv 8.0E-06 7.0E-06 7
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 8
rs75873440
RET
0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 10
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs752742313
PIK3CB
0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
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
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73