Disease: Malignant Neoplasms
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1019340046
TP53
0.882 0.080 17 7674225 missense variant C/T snv 5
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs1330189219
LTA ; LOC100287329 ; TNF
0.882 0.080 6 31573570 synonymous variant C/T snv 4.0E-06 5
rs2233947
PSORS1C2 ; PSORS1C1
0.851 0.080 6 31139278 non coding transcript exon variant C/T snv 9.3E-03 6
rs2352028
GPC5
0.851 0.080 13 91792975 intron variant C/G;T snv 6
rs383362
WWOX ; MAF
0.882 0.080 16 79211923 missense variant G/T snv 0.44 0.46 4
rs3842
ABCB1
0.882 0.080 7 87504050 3 prime UTR variant T/C snv 0.16 5
rs5744724
POLK
0.882 0.080 5 75599649 3 prime UTR variant G/C snv 5.4E-02 5
rs6183
GHR
0.827 0.080 5 42718990 missense variant C/A snv 2.3E-03 7.4E-04 8
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs12918952
WWOX
0.851 0.120 16 78386878 missense variant G/A;C;T snv 7
rs144779807
TERT
0.827 0.120 5 1268529 missense variant C/A;T snv 4.0E-06; 4.0E-05 7
rs1805076
PPP2R1B
0.851 0.120 11 111764842 missense variant C/T snv 6.5E-03 7.0E-03 7
rs1805388
LIG4
0.790 0.120 13 108211243 missense variant G/A snv 0.18 0.16 11
rs2230229
TNFRSF10A
0.807 0.120 8 23191779 missense variant C/T snv 0.88 0.86 8
rs2522137
MSI1
0.827 0.120 12 120342128 3 prime UTR variant T/A;C;G snv 7
rs25406
PCNA-AS1 ; PCNA
0.807 0.120 20 5118990 intron variant G/A snv 0.41 8
rs2602141
TP53BP1
0.790 0.120 15 43432448 missense variant T/G snv 0.36 0.47 9
rs3136797
POLB
0.827 0.120 8 42369287 missense variant C/G snv 1.1E-02 1.1E-02 10
rs33917957
MET
0.790 0.120 7 116700208 missense variant A/G snv 2.7E-02 1.8E-02 10
rs3743073
CHRNA3
0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs3757328
ZNRD1 ; ZNRD1ASP
0.851 0.120 6 30060575 non coding transcript exon variant G/A snv 9.8E-02 6