Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918457
PTPN11
0.701 0.280 12 112488466 missense variant C/T snv 4.0E-06 7.0E-06 24
rs121918467
PTPN11
0.807 0.280 12 112486482 missense variant C/A;T snv 8.0E-06; 1.2E-05 23
rs121918453
PTPN11
0.732 0.280 12 112450394 missense variant G/A;C;T snv 19
rs121918454
PTPN11
0.742 0.280 12 112450395 missense variant C/A;G;T snv 17
rs397517154
SOS1
0.763 0.280 2 39022773 missense variant C/A;G;T snv 4.0E-06 16
rs121918466
PTPN11
0.752 0.280 12 112450416 missense variant A/G snv 14
rs397507547
PTPN11
0.752 0.280 12 112489086 missense variant A/G snv 4.0E-06 14
rs121918456
PTPN11
0.752 0.280 12 112473023 missense variant A/C;G snv 13
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12
rs869025195
RIT1
0.790 0.280 1 155904493 missense variant T/G snv 11
rs121908595
MAP2K1
0.827 0.280 15 66436843 missense variant A/G snv 4.0E-06 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
rs387906660
BRAF
0.790 0.280 7 140801550 missense variant G/A;C;T 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
rs397516895
BRAF
0.827 0.280 7 140753392 missense variant A/T snv 5
rs113954997
RRAS2
0.882 0.280 11 14294844 missense variant T/A;C snv 3
rs397507531
PTPN11
0.752 0.320 12 112473040 missense variant T/C;G snv 18
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 13
rs397507542
PTPN11
0.790 0.320 12 112489069 missense variant G/T snv 9
rs121918458
PTPN11
0.807 0.320 12 112489080 missense variant T/A;G snv 8
rs730881014
RIT1
0.776 0.360 1 155904494 stop gained A/C;G;T snv 15
rs121918460
PTPN11
0.708 0.400 12 112450364 missense variant T/A;G snv 4.0E-06 27
rs672601334
RIT1
0.752 0.400 1 155904798 missense variant G/C snv 18