Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 73
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
rs104894362
KRAS
0.882 0.200 12 25209894 missense variant G/C snv 3
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
rs1057519806
MAP2K2
0.882 0.200 19 4110583 missense variant T/C snv 3
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121434497
MAP2K2
0.925 0.160 19 4117552 missense variant A/C;T snv 2
rs121434498
MAP2K2
0.807 0.280 19 4117553 missense variant A/C;G;T snv 6
rs121434499
MAP2K2
0.925 0.160 19 4110559 missense variant A/G snv 2
rs121908594
MAP2K1
0.925 0.160 15 66435104 missense variant T/C snv 2
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
rs121913337
BRAF
0.925 0.200 7 140753353 missense variant A/C;T snv 2
rs121913341
BRAF
0.851 0.280 7 140753350 missense variant A/C;T snv 5
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs121913349
BRAF
0.925 0.200 7 140781618 missense variant C/G;T snv 2
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12
rs121913375
BRAF
0.851 0.240 7 140753339 missense variant G/A;C snv 7
rs121913378
BRAF
0.776 0.280 7 140753337 missense variant C/A;G;T snv 11
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1434040739
HRAS ; LOC101059906 ; LRRC56
0.925 0.200 11 532745 missense variant T/A snv 8.1E-06 7.0E-06 2