Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 12
rs121913378
BRAF
0.776 0.280 7 140753337 missense variant C/A;G;T snv 11
rs121913368
BRAF
0.925 0.040 7 140753345 missense variant AG/GA mnv 2
rs104894095
CDKN2A
0.827 0.120 9 21971200 missense variant C/G;T snv 9.0E-06 6
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs868224085
EPHA4
1.000 0.040 2 221482474 missense variant G/A snv 1
rs267601191
EPHB4
1.000 0.040 7 100819817 missense variant G/A snv 1
rs1451501407
GUCY2D
1.000 0.040 17 8006628 missense variant G/A snv 1
rs993022333
KIT
0.851 0.080 4 54733173 missense variant A/C;T snv 5
rs1238066548
LOC105372397 ; MAP4K1
1.000 0.040 19 38595699 missense variant G/A;T snv 1
rs267601046
LOC105375064 ; TTBK1
1.000 0.040 6 43283303 missense variant C/T snv 1
rs1024708183
MAP2K7
0.925 0.040 19 7909761 missense variant A/G snv 4
rs745382803
MITF
1.000 0.040 3 69965076 missense variant C/A;G snv 4.0E-06; 4.0E-06 1
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs121913254
NRAS
0.658 0.440 1 114713909 stop gained G/A;C;T snv 31
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs907102077
OGG1 ; CAMK1
1.000 0.040 3 9760752 missense variant G/A snv 1
rs1484691555
PAK5
1.000 0.040 20 9539512 missense variant C/T snv 4.0E-06 1