Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918459
PTPN11
0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs397507520
PTPN11
0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 31
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 27
rs121918453
PTPN11
0.732 0.280 12 112450394 missense variant G/A;C;T snv 19
rs397507531
PTPN11
0.752 0.320 12 112473040 missense variant T/C;G snv 18
rs727503109
KRAS
0.752 0.320 12 25245277 missense variant T/C snv 17
rs121918454
PTPN11
0.742 0.280 12 112450395 missense variant C/A;G;T snv 17
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
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
rs397507549
PTPN11
0.742 0.240 12 112489104 missense variant C/A;G snv 13
rs121918470
PTPN11
0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 10
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
rs397507510
PTPN11
0.776 0.280 12 112450361 missense variant G/A;C;T snv 8
rs397507506
PTPN11
0.807 0.240 12 112450354 missense variant C/A;G snv 6
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
rs730880471
KRAS
0.851 0.280 12 25225709 missense variant C/T snv 4
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
rs104894364
KRAS
0.925 0.160 12 25227351 missense variant G/A snv 2