Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397516904
BRAF
0.925 0.200 7 140801487 missense variant T/C;G snv 2
rs727502904
BRAF
0.925 0.200 7 140734763 missense variant G/A;T snv 2
rs727504375
BRAF
0.925 0.200 7 140778059 missense variant T/G snv 2
rs1457537911
FGFR3
1.000 0.160 4 1801883 missense variant A/G snv 7.0E-06 2
rs1434040739
HRAS ; LOC101059906 ; LRRC56
0.925 0.200 11 532745 missense variant T/A snv 8.1E-06 7.0E-06 2
rs387907205
KRAS
0.925 0.160 12 25227313 missense variant A/C;G snv 2
rs397517042
KRAS
0.925 0.200 12 25209896 missense variant A/C;T snv 2
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
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
rs906171410
RAF1
1.000 0.160 3 12599738 missense variant C/T snv 1.6E-05 1.4E-05 2
rs180177037
BRAF
1.000 0.160 7 140778013 missense variant T/C snv 1
rs397507465
BRAF
1.000 0.160 7 140801542 missense variant T/G snv 1
rs397507470
BRAF
1.000 0.160 7 140801488 missense variant G/T snv 1
rs397507473
BRAF
1.000 0.160 7 140781605 missense variant A/G snv 4.0E-06 1
rs397507474
BRAF
1.000 0.160 7 140778061 missense variant T/C;G snv 4.0E-06 1
rs397507479
BRAF
1.000 0.160 7 140777011 missense variant C/T snv 1
rs397507480
BRAF
1.000 0.160 7 140754233 missense variant A/C snv 1
rs397507486
BRAF
1.000 0.160 7 140739813 missense variant T/C snv 1