Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 48
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
rs397517148
SOS1
0.776 0.200 2 39023128 missense variant C/T snv 27
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
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
rs672601334
RIT1
0.752 0.400 1 155904798 missense variant G/C snv 18
rs121918454
PTPN11
0.742 0.280 12 112450395 missense variant C/A;G;T snv 17
rs730881014
RIT1
0.776 0.360 1 155904494 stop gained A/C;G;T snv 15
rs121918466
PTPN11
0.752 0.280 12 112450416 missense variant A/G snv 14
rs121918456
PTPN11
0.752 0.280 12 112473023 missense variant A/C;G snv 13
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 13
rs267607079
SOS1
0.776 0.240 2 39022772 missense variant C/A;G snv 13
rs397507549
PTPN11
0.742 0.240 12 112489104 missense variant C/A;G snv 13
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 12
rs137852813
SOS1
0.807 0.200 2 39051202 missense variant A/C;G snv 11
rs869025195
RIT1
0.790 0.280 1 155904493 missense variant T/G snv 11
rs397507514
PTPN11
0.790 0.240 12 112450408 missense variant G/C;T snv 10
rs397507509
PTPN11
0.807 0.240 12 112450359 missense variant G/C;T snv 9
rs397507542
PTPN11
0.790 0.320 12 112489069 missense variant G/T snv 9
rs869025191
RIT1
0.827 0.160 1 155904739 missense variant C/A;G;T snv 9
rs121918458
PTPN11
0.807 0.320 12 112489080 missense variant T/A;G snv 8
rs180177042
BRAF
0.807 0.280 7 140749365 missense variant A/C;T snv 8
rs397507510
PTPN11
0.776 0.280 12 112450361 missense variant G/A;C;T snv 8