Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 7
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 5
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 2
rs121913341
BRAF
0.851 0.280 7 140753350 missense variant A/C;T snv 2
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 2
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 2
rs104894094
CDKN2A
0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 2
rs1064794292
CDKN2A
0.882 0.200 9 21974760 missense variant C/T snv 2
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 2
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 2
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 2
rs121913506
KIT
0.677 0.320 4 54733154 missense variant G/A;C;T snv 2
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 2
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 2
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 2
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 2
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 2