Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs1057519696
ALK
1.000 0.040 2 29214054 missense variant C/T snv 1
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 10
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 1
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 1
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 1
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 9
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 1
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 12
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 34
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 3
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 3
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 21
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 13
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 7
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 2
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 3
rs146795390
EGFR
0.827 0.080 7 55191776 missense variant G/A snv 8.0E-06 7.0E-06 1
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 2
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 4