Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
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
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs752742313
PIK3CB
0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs75873440
RET
0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 10
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 8
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
rs1057519803
ERBB3
0.925 0.080 12 56088138 missense variant G/A snv 4
rs397517096
EGFR
0.851 0.120 7 55174776 missense variant TT/CC mnv 4
rs121913247
MET
0.882 0.200 7 116783359 missense variant T/C snv 3
rs758204762
ERBB2
0.925 0.080 17 39712330 missense variant G/A;C snv 4.0E-06; 1.6E-05 2
rs1345316856
PBK ; ESCO2
1.000 0.080 8 27810979 missense variant A/C snv 4.0E-06 1
rs1452020002
ERBB4
1.000 0.080 2 211947467 missense variant G/C;T snv 1
rs4872077
TNFRSF10A
1.000 0.080 8 23200675 intron variant T/A;C snv 0.29 1