Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1441638629
GH1 ; CSHL1
0.925 0.200 17 63918773 missense variant C/T snv 4.0E-06 1.4E-05 2
rs140074469
GRAP2
1.000 0.160 22 39966148 missense variant G/A snv 7.2E-05 3.4E-04 1
rs1434040739
HRAS ; LOC101059906 ; LRRC56
0.925 0.200 11 532745 missense variant T/A snv 8.1E-06 7.0E-06 2
rs878854761
HRAS ; LRRC56
1.000 0.160 11 534319 missense variant T/C snv 1
rs745410279
IGF1
0.925 0.200 12 102478498 missense variant T/C snv 4.1E-06 2
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs727503109
KRAS
0.752 0.320 12 25245277 missense variant T/C snv 17
rs104894360
KRAS
0.724 0.560 12 25209904 missense variant T/A;C snv 14
rs104894365
KRAS
0.827 0.320 12 25245345 missense variant C/T snv 9
rs104894366
KRAS
0.776 0.400 12 25245284 missense variant G/A;C snv 9
rs104894359
KRAS
0.851 0.200 12 25227346 missense variant C/G;T snv 5
rs104894361
KRAS
0.882 0.240 12 25245370 missense variant T/A;C;G snv 4.0E-06 3
rs104894362
KRAS
0.882 0.200 12 25209894 missense variant G/C snv 3
rs727503108
KRAS
0.882 0.280 12 25227345 missense variant C/A snv 4.0E-06 3
rs727503110
KRAS
0.882 0.160 12 25245320 missense variant T/A;C snv 3
rs104894364
KRAS
0.925 0.160 12 25227351 missense variant G/A snv 2
rs193929331
KRAS
0.925 0.160 12 25245372 missense variant T/C snv 2
rs202247812
KRAS
1.000 0.160 12 25225717 missense variant T/C snv 2
rs397517042
KRAS
0.925 0.200 12 25209896 missense variant A/C;T snv 2
rs727504662
KRAS
0.925 0.160 12 25227310 missense variant T/A snv 2
rs397517041
KRAS
1.000 0.160 12 25209908 missense variant C/A snv 1
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs777243508
LZTR1
0.925 0.160 22 20993977 stop gained G/A snv 1.4E-04 1.8E-04 2