Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894094
CDKN2A
0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 2
rs104894095
CDKN2A
0.827 0.120 9 21971200 missense variant C/G;T snv 9.0E-06 1
rs104894097
CDKN2A
0.807 0.240 9 21974757 missense variant C/A;G;T snv 1.7E-05; 1.3E-05 1
rs104894098
CDKN2A
0.851 0.200 9 21970982 missense variant A/T snv 1
rs104894099
CDKN2A
0.851 0.200 9 21971183 missense variant A/C;T snv 4.6E-06 1
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 2
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
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
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 1
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 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
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
rs121913113
FGFR3
0.882 0.240 4 1806076 missense variant G/A snv 1
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 1
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 2
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 1
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 1
rs121913254
NRAS
0.658 0.440 1 114713909 stop gained G/A;C;T snv 2