Disease: Breast Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4803455
TGFB1
0.752 0.280 19 41345604 intron variant C/A snv 0.51 11
rs4808075
BABAM1 ; USHBP1
0.701 0.280 19 17279482 intron variant T/C snv 0.26 18
rs4809960
CYP24A1
0.807 0.240 20 54169534 intron variant T/C snv 0.20 8
rs481519
NEK10
0.708 0.280 3 27285723 intron variant C/A;T snv 17
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02 17
rs6022999
CYP24A1
0.790 0.160 20 54171474 intron variant A/G snv 0.36 9
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 14
rs73110464
KRT8
0.708 0.280 12 52918828 intron variant C/T snv 0.12 17
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs7725218
TERT
0.708 0.280 5 1282299 intron variant G/A snv 0.38 17
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs75316749
LOC107986051
0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 18
rs7794030 0.776 0.120 7 38712494 intergenic variant A/G snv 0.23 10
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs9834244 0.776 0.120 3 151704793 intergenic variant G/A snv 6.1E-02 10
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs1114167806
MSH2
0.827 0.200 2 47463096 stop gained ATGA/-;ATGAATGA delins 7
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs975263
MACC1
0.827 0.120 7 20158817 stop gained G/A;T snv 0.34 7
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21