Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894367
KRAS
1.000 0.160 12 25209907 missense variant A/C snv 1
rs104894364
KRAS
0.925 0.160 12 25227351 missense variant G/A snv 2
rs1135401776
KRAS
1.000 0.160 12 25225624 missense variant T/C snv 2
rs193929331
KRAS
0.925 0.160 12 25245372 missense variant T/C snv 2
rs397507512
PTPN11
0.925 0.160 12 112450391 missense variant T/C;G snv 2
rs397507518
PTPN11
0.925 0.160 12 112450508 missense variant G/A snv 2
rs397516810
PTPN11
0.925 0.160 12 112477652 missense variant T/G snv 2
rs727503380
PTPN11
0.925 0.160 12 112450386 missense variant A/T snv 2
rs574088829
SOS1
0.925 0.160 2 39012319 missense variant T/A;G snv 4.0E-06 2
rs727503110
KRAS
0.882 0.160 12 25245320 missense variant T/A;C snv 3
rs121918468
PTPN11
0.882 0.160 12 112488444 missense variant G/A;T snv 3
rs730880471
KRAS
0.851 0.280 12 25225709 missense variant C/T snv 4
rs104894359
KRAS
0.851 0.200 12 25227346 missense variant C/G;T snv 5
rs397516830
RAF1
0.827 0.160 3 12604182 missense variant A/C;G;T snv 5
rs397507506
PTPN11
0.807 0.240 12 112450354 missense variant C/A;G snv 6
rs397507510
PTPN11
0.776 0.280 12 112450361 missense variant G/A;C;T snv 8
rs104894365
KRAS
0.827 0.320 12 25245345 missense variant C/T snv 9
rs104894366
KRAS
0.776 0.400 12 25245284 missense variant G/A;C snv 9
rs121918470
PTPN11
0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 10
rs397507549
PTPN11
0.742 0.240 12 112489104 missense variant C/A;G snv 13
rs104894360
KRAS
0.724 0.560 12 25209904 missense variant T/A;C snv 14
rs121918466
PTPN11
0.752 0.280 12 112450416 missense variant A/G snv 14
rs121913496
LRRC56 ; HRAS
0.724 0.440 11 533873 missense variant C/A;G;T snv 16
rs267607048
SHOC2
0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 16
rs397517154
SOS1
0.763 0.280 2 39022773 missense variant C/A;G;T snv 4.0E-06 16