Source: UNIPROT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs193929331
KRAS
0.925 0.160 12 25245372 missense variant T/C snv 1
rs727503109
KRAS
0.752 0.320 12 25245277 missense variant T/C snv 1
rs727503110
KRAS
0.882 0.160 12 25245320 missense variant T/A;C snv 1
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 1
rs267606920
NRAS
0.882 0.160 1 114713911 missense variant C/T snv 7.0E-06 1
rs267606921
NRAS
0.882 0.160 1 114713941 missense variant G/A snv 1
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 1
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 1
rs121918458
PTPN11
0.807 0.320 12 112489080 missense variant T/A;G snv 1
rs121918459
PTPN11
0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 1
rs121918460
PTPN11
0.708 0.400 12 112450364 missense variant T/A;G snv 4.0E-06 1
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 1
rs121918463
PTPN11
0.851 0.240 12 112477651 missense variant T/A;C;G snv 1
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 1
rs121918466
PTPN11
0.752 0.280 12 112450416 missense variant A/G snv 1
rs121918469
PTPN11
0.882 0.160 12 112488454 missense variant G/C snv 1
rs121918470
PTPN11
0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 1
rs28933386
PTPN11
0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 1
rs376607329
PTPN11
0.851 0.200 12 112472981 missense variant G/A;T snv 3.2E-05 3.5E-05 1
rs397507501
PTPN11
0.882 0.160 12 112446385 missense variant A/G snv 1
rs397507506
PTPN11
0.807 0.240 12 112450354 missense variant C/A;G snv 1
rs397507509
PTPN11
0.807 0.240 12 112450359 missense variant G/C;T snv 1
rs397507514
PTPN11
0.790 0.240 12 112450408 missense variant G/C;T snv 1
rs397507517
PTPN11
0.827 0.160 12 112450497 missense variant A/C snv 1