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
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
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
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
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
rs121912532
STON1-GTF2A1L ; LHCGR ; GTF2A1L
0.776 0.280 2 48688065 missense variant C/A;G;T snv 1.2E-05 12
rs386352319
KCNJ5
0.827 0.080 11 128911724 missense variant G/A;C snv 8
rs121908864
TSHR ; LOC101928462
0.851 0.120 14 81143416 missense variant T/C;G snv 4.0E-06 6
rs104894359
KRAS
0.851 0.200 12 25227346 missense variant C/G;T snv 5
rs2069852 0.925 0.080 7 22732641 downstream gene variant G/A;C snv 4
rs28937584
TSHR ; LOC101928462
0.925 0.080 14 81143955 missense variant G/A;C snv 4.0E-06 4
rs375878504
LOC101059906 ; HRAS ; LRRC56
1.000 0.080 11 532741 synonymous variant G/A;C snv 8.1E-06 7.0E-06 3
rs1363782162
AR
X 67546155 missense variant G/A snv 5.5E-06 1
rs765808222
FGB
4 154569614 missense variant G/C snv 4.0E-06 7.0E-06 1
rs750198847
LOC101928462 ; TSHR
14 81143650 missense variant G/A snv 3.6E-05 4.2E-05 1
rs764330550
TSHR ; LOC101928462
14 81143730 missense variant G/T snv 4.0E-06 1