Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80357706
BRCA1
0.925 0.200 17 43093125 frameshift variant CA/- delins 4.0E-06 4
rs80357714
BRCA1
0.925 0.200 17 43094150 frameshift variant -/T delins 4
rs80357724
BRCA1
0.925 0.200 17 43094732 frameshift variant AA/-;A;AAA delins 4
rs80357772
BRCA1
0.925 0.200 17 43094549 frameshift variant AT/- del 4
rs80357787
BRCA1
0.925 0.200 17 43091008 frameshift variant TC/- delins 4
rs80359759
BRCA2
0.925 0.200 13 32394832 frameshift variant G/- delins 4
rs864622401
BRCA2
0.882 0.200 13 32339092 frameshift variant -/TG delins 4
rs878853297
BRCA2
0.925 0.200 13 32319166 frameshift variant AA/-;A;AAA delins 4
rs1057518636
BRCA1
1.000 17 43047646 frameshift variant -/A ins 3
rs276174819
BRCA2
0.925 0.200 13 32336524 frameshift variant -/A delins 3
rs397507396
BRCA2
0.925 0.200 13 32363405 frameshift variant CC/-;C;CCC delins 3
rs483353077
BRCA2
1.000 13 32370470 frameshift variant TTT/AAAA;NNNN delins 3
rs483353111
BRCA2
0.925 0.200 13 32336949 frameshift variant A/- delins 3
rs80357718
BRCA1
0.925 0.200 17 43071198 frameshift variant AAGAG/- delins 3
rs80357760
BRCA1
0.925 0.120 17 43063941 frameshift variant AA/-;AAA delins 3
rs80359706
BRCA2
1.000 13 32363522 frameshift variant -/T delins 3
rs1057517590
BRCA1
1.000 17 43063370 frameshift variant A/- del 2
rs1057518635
BRCA2
1.000 13 32340367 frameshift variant ATAG/- delins 2
rs1060505051
BRCA1
1.000 17 43091883 frameshift variant AAGTT/- delins 2
rs1555281594
BRCA2
1.000 13 32332276 frameshift variant -/G delins 2
rs1555282830
BRCA2
1.000 13 32337109 frameshift variant C/- del 2
rs1555460315
PALB2
1.000 0.080 16 23629673 frameshift variant GT/- delins 2
rs1555581104
BRCA1
1.000 17 43071235 frameshift variant CC/- delins 2
rs397507643
BRCA2
1.000 13 32337181 frameshift variant TTAA/- delins 2
rs397507644
BRCA2
1.000 13 32337198 frameshift variant T/- delins 2