Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 12
rs869025195
RIT1
0.790 0.280 1 155904493 missense variant T/G snv 11
rs137852813
SOS1
0.807 0.200 2 39051202 missense variant A/C;G snv 11
rs121918470
PTPN11
0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 10
rs397507514
PTPN11
0.790 0.240 12 112450408 missense variant G/C;T snv 10
rs267606706
CBL
0.807 0.240 11 119278181 missense variant T/A;C snv 8.0E-06 9
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
rs180177042
BRAF
0.807 0.280 7 140749365 missense variant A/C;T snv 8
rs121908595
MAP2K1
0.827 0.280 15 66436843 missense variant A/G snv 4.0E-06 8
rs121918458
PTPN11
0.807 0.320 12 112489080 missense variant T/A;G snv 8
rs397507510
PTPN11
0.776 0.280 12 112450361 missense variant G/A;C;T snv 8
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
rs387906660
BRAF
0.790 0.280 7 140801550 missense variant G/A;C;T snv 7
rs397517150
SOS1
0.827 0.160 2 39023118 missense variant A/C;G snv 7
rs387906661
BRAF
0.807 0.280 7 140801551 missense variant T/G snv 6
rs397507466
BRAF
0.807 0.280 7 140801537 missense variant T/A;C;G snv 4.0E-06 6
rs121918463
PTPN11
0.851 0.240 12 112477651 missense variant T/A;C;G snv 6
rs397507506
PTPN11
0.807 0.240 12 112450354 missense variant C/A;G snv 6
rs397516895
BRAF
0.827 0.280 7 140753392 missense variant A/T snv 5
rs397507501
PTPN11
0.882 0.160 12 112446385 missense variant A/G snv 5