Disease: Malignant Neoplasms
Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10012
CYP1B1 ; CYP1B1-AS1
0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 40
rs1012477
PER3
0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10175368
CYP1B1 ; CYP1B1-AS1
0.925 0.080 2 38080719 intron variant C/T snv 0.23 4
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 59
rs1034528
MTOR ; ANGPTL7
0.882 0.120 1 11189075 intron variant G/C snv 0.30 5
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs1047840
EXO1
0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs10486567
JAZF1
0.851 0.120 7 27936944 intron variant G/A snv 0.28 8
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1049216
CASP3
0.790 0.200 4 184628935 3 prime UTR variant A/G snv 0.27 9
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs10505346
COLEC10 ; TNFRSF11B
0.925 0.080 8 118951604 intron variant G/T snv 0.22 4
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1052576
CASP9
0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs1056827
CYP1B1 ; CYP1B1-AS1
0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 6
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 10
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72