Disease: Malignant neoplasm of breast
Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003623
ATM
0.925 0.080 11 108281855 intron variant C/G;T snv 2
rs1004982
LOC112268146 ; CYP19A1
0.925 0.080 15 51321614 non coding transcript exon variant T/C;G snv 2
rs10053538
HAVCR2
0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs1011329790
GGCT
0.925 0.080 7 30504681 missense variant G/A snv 3
rs10145182
NIN
0.925 0.080 14 50809291 intron variant T/A;C;G snv 2
rs10169372
LOC101928278
0.925 0.080 2 217006626 intergenic variant A/G;T snv 2
rs1029342144
KLLN ; PTEN
0.882 0.120 10 87864162 5 prime UTR variant C/G;T snv 6
rs1036980234
PTCH1
0.827 0.160 9 95447156 missense variant G/A snv 6
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 8
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042638
TPD52
0.925 0.080 8 80037711 3 prime UTR variant G/A;T snv 2
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1042821
MSH6
0.732 0.280 2 47783349 missense variant G/A;C;T snv 0.18; 8.6E-06 16
rs1042838
PGR
0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 12
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19
rs10439478
ACYP2
0.925 0.080 2 54232313 intron variant A/C;G;T snv 2
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs1044484322
CASP8
0.925 0.080 2 201271565 missense variant T/A;G snv 4.0E-06 2
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1046428
GSTZ1
0.776 0.200 14 77327940 missense variant T/A;C snv 4.0E-06; 0.81 8
rs1048249612
CHEK1
0.925 0.080 11 125629291 missense variant G/A snv 2
rs10483813
RAD51B
0.851 0.120 14 68564567 intron variant T/A;C snv 4