Disease: melanoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024708183
MAP2K7
0.925 0.040 19 7909761 missense variant A/G snv 4
rs1057519702
KIT
1.000 0.040 4 54726020 missense variant T/C snv 2
rs1057519730
MAP2K1
1.000 0.040 15 66436786 missense variant T/A;G snv 2
rs1057519804
AKT1
1.000 0.040 14 104776711 missense variant G/T snv 2
rs1057519808
MAP2K2
1.000 0.040 19 4117543 missense variant T/G snv 2
rs1057519837
CTNNB1
1.000 0.040 3 41224631 missense variant C/G;T snv 2
rs121913323
STK11
1.000 0.040 19 1220416 stop gained C/T snv 2
rs137853080
STK11
1.000 0.040 19 1207058 missense variant T/G snv 2
rs137853081
STK11
1.000 0.040 19 1219352 missense variant G/C;T snv 2
rs1487774219
CDKN2B ; CDKN2B-AS1
1.000 0.040 9 22008910 missense variant T/C snv 8.1E-06 2
rs755007339
RGS7
1.000 0.040 1 241098711 missense variant G/A;C snv 1.2E-05; 4.0E-06 2
rs765857063
RAF1
1.000 0.040 3 12618634 missense variant G/A snv 4.0E-06 7.0E-06 2
rs776761577
COL11A2
1.000 0.040 6 33179444 missense variant C/A;T snv 2.9E-05 2
rs1057519853
GNAQ
0.851 0.080 9 77794572 missense variant TG/AA mnv 6
rs1057519860
EGFR
0.851 0.080 7 55160316 missense variant C/A snv 5
rs1334613121
PRIMA1
0.925 0.080 14 93787688 missense variant C/T snv 3
rs137852789
TP53
0.925 0.080 17 7675152 missense variant C/G;T snv 4.0E-06 3.5E-05 3
rs750697353
RAF1
0.882 0.080 3 12608919 missense variant C/T snv 1.2E-05 2.8E-05 4
rs910532454
CXCR4
0.882 0.080 2 136115453 missense variant C/A;T snv 4.0E-06 4
rs1057519855
HRAS ; LRRC56
0.776 0.120 11 533873 missense variant CT/AC;TC mnv 11
rs1057519874
RAC1
0.807 0.120 7 6387261 missense variant C/A;T snv 9
rs121913512
KIT
0.851 0.120 4 54728055 missense variant A/C;G snv 9
rs121913513
KIT
0.776 0.120 4 54727495 missense variant T/C snv 10
rs121913517
KIT
0.851 0.120 4 54727444 missense variant T/A;C;G snv 6
rs121913521
KIT
0.790 0.120 4 54727447 missense variant T/A;C;G snv 12