Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs55853698
CHRNA5
0.882 0.080 15 78565597 5 prime UTR variant T/G snv 0.25 5
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 19
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs1057519879
PATL2 ; B2M
0.763 0.280 15 44711548 start lost T/C;G snv 10
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 33
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs4353229
CASP7
0.807 0.160 10 113729830 3 prime UTR variant T/C snv 0.23 6
rs36600
MTMR3
0.827 0.080 22 29941597 intron variant T/C snv 0.78 5
rs3787728
LOC100133286 ; CBR1 ; SETD4
0.851 0.080 21 36071595 intron variant T/C snv 0.74 5
rs397517097
EGFR
0.851 0.080 7 55174777 missense variant T/C snv 4
rs1045494
CASP8
0.882 0.120 2 201287058 3 prime UTR variant T/C snv 0.10 3
rs942190
TDP1 ; EFCAB11
1.000 0.080 14 89956320 intron variant T/C snv 0.37 2
rs114033761 1.000 0.080 6 31093784 regulatory region variant T/C snv 1
rs117729306
STK33
1.000 0.080 11 8465623 non coding transcript exon variant T/C snv 7.3E-03 1
rs140013431
BMP6
1.000 0.080 6 7770278 intron variant T/C snv 1.2E-02 1
rs1778335
PIP4K2A
1.000 0.080 10 22643219 intron variant T/C snv 0.27 1
rs3134425
CRTAM
1.000 0.080 11 122838470 intron variant T/C snv 0.67 1
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88