Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 2
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 1
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 2
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 5
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 3
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs1064794292
CDKN2A
0.882 0.200 9 21974760 missense variant C/T snv 2
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 2
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 2
rs121913254
NRAS
0.658 0.440 1 114713909 stop gained G/A;C;T snv 2
rs121913315
STK11
0.882 0.160 19 1220488 missense variant G/A;T snv 2
rs121913341
BRAF
0.851 0.280 7 140753350 missense variant A/C;T snv 2
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;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
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 2
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 2
rs104894098
CDKN2A
0.851 0.200 9 21970982 missense variant A/T snv 1
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs104894340
CDK4
0.827 0.200 12 57751647 missense variant C/A;T snv 1
rs1057519713
KIT
0.925 0.120 4 54736498 missense variant G/C snv 1
rs121909233
KLLN ; PTEN
1.000 0.040 10 87864524 missense variant G/A snv 1
rs121909234
PTEN
1.000 0.040 10 87957867 missense variant G/A snv 1