Disease: cervical cancer
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs1049216
CASP3
0.790 0.200 4 184628935 3 prime UTR variant A/G snv 0.27 9
rs9298814
IFNA17
0.790 0.160 9 21227623 missense variant A/C;G snv 0.12; 8.8E-06 7
rs13117307
EXOC1
0.827 0.080 4 55885574 intron variant C/T snv 0.21 6
rs4282438
COL11A2P1
0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 6
rs750553272
NFE2L2
0.851 0.080 2 177230898 missense variant G/A snv 1.2E-05 7.0E-06 4
rs9277952 0.851 0.080 6 33236497 upstream gene variant G/A snv 0.10 4