Source: UNIPROT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 5
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 2
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 2
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 2
rs397507520
PTPN11
0.658 0.520 12 112453279 missense variant G/C;T snv 1
rs121918459
PTPN11
0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 1
rs80338796
RAF1
0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 2
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 1
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 1
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 1
rs397507545
PTPN11
0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06 2
rs121918460
PTPN11
0.708 0.400 12 112450364 missense variant T/A;G snv 4.0E-06 1
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 1
rs121918453
PTPN11
0.732 0.280 12 112450394 missense variant G/A;C;T snv 2
rs121918454
PTPN11
0.742 0.280 12 112450395 missense variant C/A;G;T snv 2
rs397507549
PTPN11
0.742 0.240 12 112489104 missense variant C/A;G snv 2
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 1
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 1
rs121918456
PTPN11
0.752 0.280 12 112473023 missense variant A/C;G snv 2
rs121918466
PTPN11
0.752 0.280 12 112450416 missense variant A/G snv 1
rs137852814
SOS1
0.752 0.240 2 39022774 missense variant T/A;C snv 4.0E-06 1
rs267607048
SHOC2
0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 1
rs28933386
PTPN11
0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 1
rs397507531
PTPN11
0.752 0.320 12 112473040 missense variant T/C;G snv 1