Disease: melanoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs765857063
RAF1
1.000 0.040 3 12618634 missense variant G/A snv 4.0E-06 7.0E-06 2
rs1057519702
KIT
1.000 0.040 4 54726020 missense variant T/C snv 2
rs1057519710
KIT
0.695 0.280 4 54733166 missense variant G/C;T snv 22
rs121913506
KIT
0.677 0.320 4 54733154 missense variant G/A;C;T snv 24
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
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 12
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
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2536512
SOD3
0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs777980327
APC
0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06 21
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs776761577
COL11A2
1.000 0.040 6 33179444 missense variant C/A;T snv 2.9E-05 2
rs1057519860
EGFR
0.851 0.080 7 55160316 missense variant C/A snv 5
rs1057519874
RAC1
0.807 0.120 7 6387261 missense variant C/A;T snv 9
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24