Disease: Malignant neoplasm of breast
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2242652
TERT
0.724 0.400 5 1279913 intron variant G/A snv 0.18 16
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs28360317
XRCC4
0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs3104746
CASC16
0.790 0.120 16 52567188 intron variant T/A snv 8.6E-02 7
rs3136817
APEX1 ; OSGEP
0.732 0.280 14 20456275 intron variant T/C snv 0.23 12
rs3731239
CDKN2A
0.763 0.240 9 21974219 intron variant A/G snv 0.26 10
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs3813867
LOC107984284 ; CYP2E1
0.732 0.240 10 133526101 intron variant G/A;C snv 13
rs3816358
ARNTL
0.827 0.120 11 13369925 intron variant C/A;T snv 5
rs3816360
ARNTL
0.807 0.120 11 13346203 intron variant T/C snv 0.58 6
rs3817198
LSP1
0.790 0.280 11 1887776 intron variant T/C snv 0.26 8
rs4246742
TERT
0.827 0.120 5 1267241 intron variant T/A snv 0.23 5
rs4645981
CASP9 ; DNAJC16
0.790 0.160 1 15524988 intron variant G/A;C snv 11
rs4808075
BABAM1 ; USHBP1
0.701 0.280 19 17279482 intron variant T/C snv 0.26 18
rs5744533
POLK ; CERT1
0.807 0.120 5 75510279 intron variant C/A;T snv 6
rs5751129
XRCC6 ; DESI1
0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs624366
ATM
0.827 0.120 11 108283370 intron variant G/C snv 0.52 6
rs6413432
CYP2E1
0.827 0.120 10 133535040 intron variant T/A snv 9.9E-02 5
rs664677
ATM
0.807 0.160 11 108272455 intron variant C/A;T snv 0.65 8
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs6869366
XRCC4 ; TMEM167A
0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 9
rs762551
CYP1A2
0.701 0.400 15 74749576 intron variant C/A snv 0.67 23