Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28897672
BRCA1
0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 16
rs41293459
BRCA1
0.763 0.280 17 43063930 missense variant C/A;G;T snv 2.4E-05 12
rs28897696
BRCA1
0.807 0.200 17 43063903 missense variant G/A;C;T snv 2.8E-05; 4.0E-06; 2.0E-05 11
rs80356898
BRCA1
0.752 0.200 17 43093844 stop gained G/A;C snv 2.8E-05; 4.0E-06 11
rs80357382
BRCA1
0.763 0.240 17 43106457 missense variant T/C snv 4.0E-06 11
rs55770810
BRCA1
0.763 0.280 17 43063931 missense variant G/A;T snv 2.4E-05; 8.0E-06 10
rs41293463
BRCA1
0.790 0.280 17 43051071 missense variant A/C;T snv 1.2E-05 9
rs80356952
BRCA1
0.790 0.200 17 43093901 stop gained G/A snv 9
rs62625307
BRCA1
0.827 0.200 17 43091933 stop gained G/A snv 4.0E-06 8
rs62625308
BRCA1
0.851 0.200 17 43091924 stop gained G/A;C snv 1.2E-05 8
rs80356962
BRCA1
0.807 0.200 17 43047666 stop gained C/G;T snv 4.0E-06 7.0E-06 8
rs80357086
BRCA1
0.851 0.200 17 43106480 stop gained A/G;T snv 8
rs80357115
BRCA1
0.790 0.200 17 43092597 stop gained A/C;T snv 8
rs45553935
BRCA1
0.851 0.200 17 43057122 missense variant A/C;G;T snv 7
rs80356913
BRCA1
0.851 0.200 17 43106456 missense variant C/A;G;T snv 7
rs80356978
BRCA1
0.827 0.200 17 43092809 stop gained C/A;T snv 7
rs80357123
BRCA1
0.827 0.200 17 43057078 stop gained G/A;C;T snv 1.2E-05 7
rs80358044
BRCA1
0.827 0.200 17 43074330 splice donor variant C/A;G;T snv 7
rs1800709
BRCA1
0.851 0.160 17 43093010 missense variant G/A snv 1.7E-03 1.4E-03 6
rs41293455
BRCA1
0.827 0.200 17 43082434 stop gained G/A;C snv 2.4E-05; 3.2E-05 6
rs41293465
BRCA1
0.851 0.200 17 43045767 stop gained G/A snv 1.2E-05 6
rs80356885
BRCA1
0.827 0.200 17 43074482 stop gained C/T snv 6
rs80356991
BRCA1
0.882 0.200 17 43104136 stop gained C/A;G;T snv 8.4E-05 6
rs80357106
BRCA1
0.827 0.200 17 43092212 stop gained C/A snv 6
rs80357268
BRCA1
0.827 0.200 17 43045773 missense variant C/T snv 4.0E-06 6