Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918470
PTPN11
0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 10
rs869025191
RIT1
0.827 0.160 1 155904739 missense variant C/A;G;T snv 9
rs397507517
PTPN11
0.827 0.160 12 112450497 missense variant A/C snv 8
rs397507539
PTPN11
0.851 0.160 12 112489047 missense variant C/A;G;T snv 4.0E-06 8
rs397507540
PTPN11
0.851 0.160 12 112489048 missense variant C/A;T snv 8
rs397517150
SOS1
0.827 0.160 2 39023118 missense variant A/C;G snv 7
rs397507501
PTPN11
0.882 0.160 12 112446385 missense variant A/G snv 5
rs397507529
PTPN11
0.851 0.160 12 112473031 missense variant A/G snv 7.0E-06 5
rs397507541
PTPN11
0.827 0.160 12 112489068 missense variant C/T snv 4.0E-06 7.0E-06 5
rs727505381
SOS1
0.925 0.160 2 39013523 missense variant A/G snv 4.0E-06 5
rs1557962794
RIT1
0.882 0.160 1 155910693 missense variant T/G snv 4
rs267606920
NRAS
0.882 0.160 1 114713911 missense variant C/T snv 7.0E-06 4
rs267606921
NRAS
0.882 0.160 1 114713941 missense variant G/A 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
rs876657651
MAP2K1
0.882 0.160 15 66436818 missense variant A/G snv 3
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
rs606231228
BRAF
0.925 0.160 7 140777013 missense variant C/A;G snv 2
rs869025573
NRAS
1.000 0.160 1 114716090 missense variant A/T snv 2
rs869320687
SOS2
0.925 0.160 14 50161551 missense variant G/C snv 2
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