Source: UNIPROT ×
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 2
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs104894359
KRAS
0.851 0.200 12 25227346 missense variant C/G;T snv 2
rs104894361
KRAS
0.882 0.240 12 25245370 missense variant T/A;C;G snv 4.0E-06 1
rs104894364
KRAS
0.925 0.160 12 25227351 missense variant G/A snv 1
rs104894365
KRAS
0.827 0.320 12 25245345 missense variant C/T snv 1
rs104894366
KRAS
0.776 0.400 12 25245284 missense variant G/A;C snv 2
rs121434594
RAF1
0.827 0.160 3 12604189 missense variant G/A;C;T snv 1
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-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
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 1
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 2
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 1
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 5
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
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 1
rs121918456
PTPN11
0.752 0.280 12 112473023 missense variant A/C;G snv 2
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
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 2
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