Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs730881602
BRCA2
0.925 0.200 13 32336731 frameshift variant -/A delins 3
rs730881606
BRCA2
0.925 0.200 13 32338466 frameshift variant -/A delins 3
rs752780954
BRIP1
0.925 0.200 17 61686008 frameshift variant -/A delins 4.8E-05 1.4E-05 3
rs775537066
BRIP1
0.925 0.200 17 61776487 frameshift variant -/A delins 8.0E-06 2.1E-05 3
rs80357519
BRCA1
0.925 0.200 17 43092695 frameshift variant -/A delins 4.0E-06 3
rs80357687
BRCA1
0.925 0.200 17 43091771 frameshift variant -/A delins 3
rs80357932
BRCA1
0.925 0.200 17 43093638 frameshift variant -/A delins 3
rs80359335
BRCA2
0.925 0.200 13 32336936 frameshift variant -/A delins 7.0E-06 3
rs80359438
BRCA2
0.925 0.200 13 32338630 frameshift variant -/A delins 3
rs80359527
BRCA2
0.925 0.200 13 32340035 stop gained -/A delins 3
rs80359656
BRCA2
0.925 0.200 13 32356516 frameshift variant -/A delins 3
rs80359676
BRCA2
0.925 0.200 13 32357842 frameshift variant -/A delins 3
rs863224510
BRCA1
0.925 0.200 17 43093487 frameshift variant -/A delins 3
rs876659767
BRCA2
0.925 0.200 13 32337070 frameshift variant -/A delins 3
rs886040027
BRCA1
0.925 0.200 17 43093184 frameshift variant -/A delins 3
rs886040416
BRCA2
0.925 0.200 13 32336605 frameshift variant -/A delins 3
rs886040578
BRCA2
0.925 0.200 13 32339570 stop gained -/A delins 3
rs886040732
BRCA2
0.925 0.200 13 32362580 frameshift variant -/A delins 3
rs1057516541
ATM
1.000 0.200 11 108284359 frameshift variant -/A delins 2
rs1114167632
PTEN
1.000 0.080 10 87952136 frameshift variant -/A delins 2
rs1114167815
MSH2
1.000 0.160 2 47475100 frameshift variant -/A delins 2
rs1131690837
FLCN ; MPRIP
1.000 0.080 17 17216466 frameshift variant -/A delins 2
rs1405341259
BRCA2
1.000 0.200 13 32394759 frameshift variant -/A delins 4.0E-06 1.4E-05 2
rs1553644815
BAP1
1.000 3 52403449 frameshift variant -/A delins 2
rs1554898084
PTEN
1.000 0.080 10 87933059 frameshift variant -/A delins 2