Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
rs121913535
KRAS
0.742 0.320 12 25245348 missense variant C/A;G;T snv 14
rs13010627
CASP10
0.807 0.280 2 201209375 missense variant G/A snv 4.2E-02 4.3E-02 10
rs1564691414
FAS
0.925 0.160 10 89007698 splice acceptor variant A/G snv 7
rs757333753
RAF1
0.851 0.200 3 12618681 missense variant C/A;T snv 4.0E-06 6
rs17860403
CASP10
0.882 0.160 2 201208114 missense variant C/T snv 2.4E-05 2.0E-04 3
rs121913080
FAS
0.882 0.160 10 89014191 missense variant G/C snv 3
rs770692189
BCL2L11 ; MIR4435-2HG
1.000 0.120 2 111123957 missense variant G/A;T snv 1.6E-05; 4.0E-06 2
rs80358239
CASP10
0.925 0.160 2 201209363 missense variant A/C;T snv 4.5E-03 2
rs121913076
FAS
0.925 0.120 10 89014163 missense variant A/C snv 2
rs121913078
FAS
0.925 0.120 10 89008915 missense variant C/T snv 4.0E-06 2
rs121913081
FAS
0.925 0.120 10 89014251 missense variant C/T snv 2
rs121913086
FAS
0.925 0.120 10 89014220 missense variant G/T snv 2
rs1564696849
FAS
0.925 0.160 10 89012082 splice donor variant G/A snv 2
rs28929498
FAS
0.925 0.120 10 89014221 missense variant A/T snv 2
rs17860405
CASP10
1.000 0.120 2 201209484 missense variant A/G snv 3.0E-02 2.9E-02 1
rs1477247624
CASP8
1.000 0.120 2 201285277 missense variant A/C snv 4.0E-06 1
rs121913079
FAS
1.000 0.120 10 89014137 missense variant A/G snv 1
rs201072885
FAS
1.000 0.120 10 89014164 missense variant C/A snv 6.0E-05 1
rs962954379
PPIG
1.000 0.120 2 169636474 missense variant A/C snv 1.4E-05 1