Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104886028
KRAS
1.000 0.080 12 25227308 missense variant C/T snv 1
rs104894359
KRAS
0.851 0.200 12 25227346 missense variant C/G;T snv 5
rs104894360
KRAS
0.724 0.560 12 25209904 missense variant T/A;C snv 14
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
rs104894364
KRAS
0.925 0.160 12 25227351 missense variant G/A snv 2
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
rs104894367
KRAS
1.000 0.160 12 25209907 missense variant A/C snv 1
rs1057519725
KRAS
0.851 0.320 12 25225627 missense variant G/A snv 7.0E-06 6
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs1135401776
KRAS
1.000 0.160 12 25225624 missense variant T/C snv 2
rs1137188
KRAS
1.000 0.080 12 25206418 3 prime UTR variant G/A snv 0.49 2
rs1137282
KRAS
0.851 0.120 12 25209843 missense variant A/G;T snv 0.19 5
rs121913236
KRAS
0.882 0.160 12 25245321 missense variant G/C;T snv 4
rs121913238
KRAS
0.732 0.240 12 25227343 missense variant G/C;T snv 17
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913527
KRAS
0.807 0.320 12 25225628 missense variant C/A;G;T snv 9
rs121913528
KRAS
0.851 0.160 12 25227349 missense variant C/A;T snv 12
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs121913535
KRAS
0.742 0.320 12 25245348 missense variant C/A;G;T snv 14
rs121913538
KRAS
0.882 0.080 12 25245328 missense variant C/A;G snv 3
rs12587
KRAS
0.827 0.200 12 25205894 3 prime UTR variant T/G snv 0.49 5
rs1463850736
KRAS
12 25225676 missense variant C/A;G;T snv 4.0E-06 1