Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507466
BRAF
0.807 0.280 7 140801537 missense variant T/A;C;G snv 4.0E-06 6
rs397516792
MAP2K1
0.827 0.280 15 66436825 missense variant C/A;G;T snv 6
rs727504317
MAP2K1
0.807 0.320 15 66435145 missense variant G/A snv 6
rs121434498
MAP2K2
0.807 0.280 19 4117553 missense variant A/C;G;T snv 6
rs121913341
BRAF
0.851 0.280 7 140753350 missense variant A/C;T snv 5
rs180177041
BRAF
0.851 0.240 7 140777006 missense variant C/G snv 5
rs397516895
BRAF
0.827 0.280 7 140753392 missense variant A/T snv 5
rs869025340
BRAF
0.925 0.160 7 140777032 missense variant A/C;G;T snv 5
rs104894359
KRAS
0.851 0.200 12 25227346 missense variant C/G;T snv 5
rs180177038
BRAF
0.851 0.200 7 140778007 missense variant C/G;T snv 4
rs397507476
BRAF
0.882 0.200 7 140778011 missense variant T/A;G snv 4
rs397507481
BRAF
0.882 0.240 7 140754206 missense variant G/C;T snv 4
rs180177034
BRAF
0.882 0.200 7 140801536 missense variant C/G snv 3
rs397507469
BRAF
0.882 0.200 7 140801503 missense variant G/T snv 3
rs397516893
BRAF
0.925 0.160 7 140778048 missense variant A/C snv 3
rs794729219
BRAF
0.882 0.240 7 140753352 missense variant A/G snv 3
rs104894362
KRAS
0.882 0.200 12 25209894 missense variant G/C snv 3
rs727503108
KRAS
0.882 0.280 12 25227345 missense variant C/A snv 4.0E-06 3
rs1057519806
MAP2K2
0.882 0.200 19 4110583 missense variant T/C snv 3
rs397517147
SOS1
0.882 0.200 2 39023131 missense variant C/T snv 4.0E-06 3
rs121913337
BRAF
0.925 0.200 7 140753353 missense variant A/C;T snv 2
rs121913349
BRAF
0.925 0.200 7 140781618 missense variant C/G;T snv 2
rs180177036
BRAF
0.925 0.200 7 140778053 missense variant C/A;G snv 2
rs397507475
BRAF
0.925 0.200 7 140778054 missense variant A/G snv 2
rs397516903
BRAF
0.925 0.200 7 140801533 missense variant A/C;G snv 2