Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057517565
BRCA2
0.925 0.200 13 32338925 frameshift variant TTTC/- del 2
rs1057517566
BRCA2
0.925 0.200 13 32337431 frameshift variant AA/- del 2
rs1057517572
BRCA2
0.925 0.200 13 32319315 frameshift variant -/T delins 2
rs1057517595
BRCA2
1.000 13 32339841 frameshift variant GT/- delins 1
rs1057517636
BRCA2
1.000 13 32338829 stop gained A/T snv 1
rs1057517865
BRCA2
1.000 13 32371025 stop gained A/T snv 1
rs1057518635
BRCA2
1.000 13 32340367 frameshift variant ATAG/- delins 2
rs1057518637
BRCA2
1.000 13 32336621 stop gained C/G;T snv 3
rs1057518638
BRCA2
1.000 13 32339317 stop gained T/A snv 2
rs1057519559
BRCA2
0.925 0.200 13 32339514 frameshift variant AACA/- delins 2
rs1057520636
BRCA2
1.000 13 32338581 stop gained T/A snv 1
rs1060499566
BRCA2
1.000 13 32316421 splice acceptor variant G/A snv 1
rs1060499833
BRCA2
1.000 13 32339338 stop gained T/G snv 1
rs1060502385
BRCA2
0.925 0.200 13 32332376 frameshift variant GTA/TT delins 2
rs1060502391
BRCA2
0.925 0.200 13 32337329 frameshift variant A/- delins 2
rs1060502392
BRCA2
0.925 0.200 13 32340925 frameshift variant A/- delins 2
rs1060502395
BRCA2
0.925 0.200 13 32326146 frameshift variant G/- del 2
rs1060502400
BRCA2
0.925 0.200 13 32340575 frameshift variant C/- del 2
rs1060502403
BRCA2
0.925 0.200 13 32332670 frameshift variant C/- del 2
rs1060502414
BRCA2
0.925 0.200 13 32336945 stop gained C/T snv 2
rs1060502426
BRCA2
0.925 0.200 13 32338628 frameshift variant G/- del 2
rs1060502433
BRCA2
0.925 0.200 13 32357846 stop gained G/A;T snv 3
rs1060502437
BRCA2
0.925 0.200 13 32336827 frameshift variant A/- delins 2
rs1060502444
BRCA2
0.925 0.200 13 32340428 frameshift variant TC/- delins 2
rs1060502449
BRCA2
0.925 0.200 13 32337461 stop gained G/A;T snv 3