Disease: Nasopharyngeal carcinoma
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 25
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 19
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 16
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs55832599
TP53
0.716 0.360 17 7673821 missense variant G/A snv 13
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs1131691003
TP53
0.752 0.360 17 7676381 splice donor variant C/A;G snv 12
rs1131691042
TP53
0.752 0.360 17 7675052 splice donor variant C/T snv 12
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 11
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 11
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 11
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22 10
rs10795668
LOC105376400
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 10
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 10
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 10
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 10
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 10
rs9929218
CDH1
0.732 0.160 16 68787043 intron variant G/A snv 0.28 10