Source: CURATED

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 10
rs80357522
BRCA1
0.776 0.280 17 43093570 frameshift variant TTTT/-;TT;TTT;TTTTT delins 7.0E-06 10
rs80356898
BRCA1
0.752 0.200 17 43093844 stop gained G/A;C snv 2.8E-05; 4.0E-06 9
rs55770810
BRCA1
0.763 0.280 17 43063931 missense variant G/A;T snv 2.4E-05; 8.0E-06 7
rs80357382
BRCA1
0.763 0.240 17 43106457 missense variant T/C snv 4.0E-06 7
rs80357906
BRCA1
0.827 0.200 17 43057062 frameshift variant -/G delins 1.8E-04 7
rs41293459
BRCA1
0.763 0.280 17 43063930 missense variant C/A;G;T snv 2.4E-05 5
rs80357474
BRCA1
0.827 0.200 17 43049188 missense variant A/C;G;T snv 8.0E-06 5
rs80357678
BRCA1
0.851 0.200 17 43091614 frameshift variant AA/- del 5
rs41293463
BRCA1
0.790 0.280 17 43051071 missense variant A/C;T snv 1.2E-05 4
rs80356959
BRCA1
0.851 0.200 17 43045761 missense variant A/C;G snv 4
rs80357086
BRCA1
0.851 0.200 17 43106480 stop gained A/G;T snv 4
rs1800751
BRCA1
0.851 0.160 17 43047676 missense variant G/A;C snv 4.0E-06 3
rs397508986
BRCA1
0.807 0.280 17 43092919 frameshift variant G/AA delins 3
rs80356932
BRCA1
0.851 0.200 17 43076600 stop gained G/A snv 3
rs80356936
BRCA1
0.851 0.200 17 43104260 stop gained A/C;G;T snv 4.0E-06 3
rs80357164
BRCA1
0.851 0.200 17 43115745 missense variant A/C;G;T snv 3
rs80357307
BRCA1
0.851 0.200 17 43045760 stop gained C/T snv 3
rs863224765
BRCA1
0.851 0.200 17 43051086 missense variant C/A;G snv 3
rs397509171
BRCA1
0.851 0.200 17 43076573 stop gained G/A snv 2
rs397509205
BRCA1
0.882 0.080 17 43070984 stop gained C/A snv 2
rs748876625
BRCA1
0.807 0.160 17 43104122 missense variant C/A;G snv 1.2E-05 2
rs786202998
BRCA1
0.851 0.080 17 43091030 stop gained C/A;T snv 2
rs80356914
BRCA1
0.851 0.200 17 43045759 stop gained C/A;G;T snv 2
rs80357112
BRCA1
0.882 0.080 17 43051063 missense variant C/A;G;T snv 2