Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 29
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs1799939
RET
0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21 27
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 27
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 24
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs121913238
KRAS
0.732 0.240 12 25227343 missense variant G/C;T snv 17
rs121913283
PIK3CA
0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 16
rs121913496
LRRC56 ; HRAS
0.724 0.440 11 533873 missense variant C/A;G;T snv 16
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs121913535
KRAS
0.742 0.320 12 25245348 missense variant C/A;G;T snv 14
rs587777790
PIK3CA
0.732 0.280 3 179199690 missense variant G/A snv 14
rs1057519736
IDH2
0.752 0.160 15 90088605 missense variant C/G snv 13
rs1207011218
CTLA4
0.742 0.440 2 203870794 synonymous variant C/T snv 12
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 12
rs1057519936
PIK3CA
0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937
PIK3CA
0.776 0.200 3 179234285 missense variant T/C snv 11
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 10
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs2227869
ERCC5 ; BIVM-ERCC5
0.790 0.240 13 102862735 missense variant G/A;C snv 4.3E-02 9