Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs564251686
PLAAT4
1.000 0.160 11 63544632 missense variant G/A snv 4.4E-05 6.3E-05 1
rs201787206
PTPN11
1.000 0.160 12 112477722 missense variant A/G snv 5.0E-04 2.5E-04 1
rs397507524
PTPN11
1.000 0.160 12 112472949 inframe insertion ACA/-;ACAACA delins 1
rs397507526
PTPN11
1.000 0.160 12 112472972 missense variant T/A;G snv 1
rs397516797
PTPN11
1.000 0.160 12 112502222 missense variant C/T snv 4.0E-05 7.0E-05 1
rs765642157
PTPN11
1.000 0.160 12 112472969 missense variant T/A;G snv 4.0E-06 1
rs80338836
PTPN11
1.000 0.160 12 112450357 inframe deletion GTG/- delins 1
rs869025574
PTPN11
1.000 0.160 12 112450360 inframe deletion GAT/- delins 1
rs886043790
PTPN11
1.000 0.160 12 112450355 missense variant A/G snv 4.0E-06 7.0E-06 1
rs606231228
BRAF
0.925 0.160 7 140777013 missense variant C/A;G snv 2
rs397514553
NRAS
0.925 0.200 1 114716060 missense variant G/A snv 2
rs869025573
NRAS
1.000 0.160 1 114716090 missense variant A/T snv 2
rs397507504
PTPN11
0.925 0.160 12 112450346 missense variant A/G snv 7.0E-06 2
rs397507525
PTPN11
0.925 0.160 12 112472968 missense variant C/T snv 7.0E-06 2
rs397507543
PTPN11
0.925 0.160 12 112489078 missense variant G/A snv 2
rs397516801
PTPN11
0.925 0.160 12 112450389 missense variant A/G snv 2
rs869320687
SOS2
0.925 0.160 14 50161551 missense variant G/C snv 2
rs180177034
BRAF
0.882 0.200 7 140801536 missense variant C/G snv 3
rs876657651
MAP2K1
0.882 0.160 15 66436818 missense variant A/G snv 3
rs267606921
NRAS
0.882 0.160 1 114713941 missense variant G/A snv 3
rs397507511
PTPN11
0.882 0.240 12 112450385 missense variant G/A;C snv 3
rs397507523
PTPN11
0.882 0.160 12 112472954 missense variant A/G snv 3
rs672601335
RIT1
0.882 0.160 1 155904456 missense variant C/G snv 3
rs113954997
RRAS2
0.882 0.280 11 14294844 missense variant T/A;C snv 3
rs267606920
NRAS
0.882 0.160 1 114713911 missense variant C/T snv 7.0E-06 4