Disease: Malignant neoplasm of breast
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs709816
NBN
0.752 0.320 8 89955483 synonymous variant A/G snv 0.47 0.51 10
rs7726159
TERT
0.790 0.160 5 1282204 intron variant C/A snv 0.29 10
rs10511729
LOC101929563
0.742 0.240 9 23557229 intron variant T/G snv 0.35 11
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs12683422
LINGO2
0.742 0.240 9 27969442 intron variant C/T snv 5.7E-02 11
rs1805388
LIG4
0.790 0.120 13 108211243 missense variant G/A snv 0.18 0.16 11
rs3754093
EXO1
0.776 0.240 1 241846814 upstream gene variant A/G snv 0.23 11
rs4645981
CASP9 ; DNAJC16
0.790 0.160 1 15524988 intron variant G/A;C snv 11
rs941759532
ERCC4
0.763 0.240 16 13932175 missense variant C/G snv 11
rs2073498
RASSF1
0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02 12
rs2470890
CYP1A2
0.742 0.320 15 74755085 synonymous variant T/C snv 0.57 12
rs3136817
APEX1 ; OSGEP
0.732 0.280 14 20456275 intron variant T/C snv 0.23 12
rs560191
TP53BP1
0.763 0.280 15 43475576 missense variant G/C;T snv 0.36; 4.0E-06 12
rs6068816
CYP24A1
0.752 0.200 20 54164552 synonymous variant C/T snv 0.12 8.9E-02 12
rs931127
SIPA1 ; PCNX3
0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs1625895
TP53
0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs2075686
TMEM167A ; XRCC4
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02 13
rs2228526
ERCC6
0.752 0.200 10 49470671 missense variant T/C snv 0.22 0.19 13
rs3813867
LOC107984284 ; CYP2E1
0.732 0.240 10 133526101 intron variant G/A;C snv 13
rs851797
EXO1
0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs104894360
KRAS
0.724 0.560 12 25209904 missense variant T/A;C snv 14
rs132770
DESI1 ; XRCC6
0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs2075685
TMEM167A ; XRCC4
0.724 0.320 5 83076846 intron variant G/A;T snv 14
rs2233678
PIN1 ; LOC100996288
0.732 0.360 19 9834503 non coding transcript exon variant G/A;C snv 14