Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434498
MAP2K2
0.807 0.280 19 4117553 missense variant A/C;G;T snv 6
rs1057519806
MAP2K2
0.882 0.200 19 4110583 missense variant T/C snv 3
rs121434497
MAP2K2
0.925 0.160 19 4117552 missense variant A/C;T snv 2
rs121434499
MAP2K2
0.925 0.160 19 4110559 missense variant A/G snv 2
rs267607230
MAP2K2
0.925 0.160 19 4110576 missense variant G/A;C;T snv 2
rs727504370
MAP2K2
0.925 0.200 19 4110558 missense variant T/C snv 2
rs727504382
MAP2K2
0.925 0.200 19 4101105 missense variant C/T snv 2
rs730880517
MAP2K2
1.000 0.160 19 4117541 missense variant T/C snv 1
rs869025608
MAP2K1
0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs121908595
MAP2K1
0.827 0.280 15 66436843 missense variant A/G snv 4.0E-06 8
rs121908596
MAP2K1
0.807 0.240 15 66436837 missense variant G/A;T snv 7
rs397516792
MAP2K1
0.827 0.280 15 66436825 missense variant C/A;G;T snv 6
rs727504317
MAP2K1
0.807 0.320 15 66435145 missense variant G/A snv 6
rs121908594
MAP2K1
0.925 0.160 15 66435104 missense variant T/C snv 2
rs397516790
MAP2K1
0.925 0.200 15 66435115 missense variant A/C;G snv 2
rs397516793
MAP2K1
0.925 0.160 15 66436842 missense variant T/C snv 2
rs797044593
MAP2K1
0.925 0.160 15 66436759 missense variant A/G snv 2
rs397516789
MAP2K1
1.000 0.160 15 66435070 missense variant C/T snv 1
rs397516791
MAP2K1
1.000 0.160 15 66435221 missense variant T/G snv 1
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
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