Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs730881939
RAD51C
0.851 0.200 17 58695008 stop gained -/A delins 5
rs1060503764
SDHB
0.925 0.080 1 17022655 frameshift variant -/A delins 4
rs1135401927
BRCA2
0.882 0.200 13 32376691 frameshift variant -/A delins 4
rs587780236
BRIP1
0.882 0.280 17 61743118 frameshift variant -/A delins 8.0E-06 7.0E-06 4
rs80359328
BRCA2
0.882 0.240 13 32336684 frameshift variant -/A delins 4
rs80359773
BRCA2
0.882 0.280 13 32398184 frameshift variant -/A delins 4
rs1057518636
BRCA1
1.000 17 43047646 frameshift variant -/A ins 3
rs1131691041
TP53
17 7676271 frameshift variant -/A delins 3
rs1553619976
VHL
0.925 0.160 3 10146593 frameshift variant -/A delins 3
rs1555618709
BRIP1
0.925 0.240 17 61861461 frameshift variant -/A delins 3
rs267608118
MSH6 ; FBXO11
1.000 0.160 2 47806453 frameshift variant -/A delins 3
rs267608156
PMS2
1.000 0.160 7 5989867 frameshift variant -/A delins 3
rs397507286
BRCA2
0.925 0.200 13 32336831 frameshift variant -/A delins 7.0E-06 3
rs397507334
BRCA2
0.925 0.200 13 32338824 frameshift variant -/A delins 4.0E-06 3
rs397507683
BRCA2
0.925 0.200 13 32338103 frameshift variant -/A delins 3
rs397507826
BRCA2
0.925 0.200 13 32340432 frameshift variant -/A delins 3
rs398122789
BRCA2
0.925 0.200 13 32339318 stop gained -/A delins 3
rs587780670
FBXO11 ; MSH6
1.000 0.160 2 47799772 frameshift variant -/A delins 3
rs587781299
ATM ; C11orf65
0.925 0.280 11 108327665 frameshift variant -/A delins 3
rs587781487
BRCA1
0.925 0.200 17 43099809 frameshift variant -/A delins 3
rs587781554
MLH1
1.000 0.160 3 37020395 frameshift variant -/A delins 3
rs587782111
FBXO11 ; MSH6
1.000 0.160 2 47804946 stop gained -/A delins 3
rs587782392
BRCA1
0.925 0.200 17 43071114 frameshift variant -/A delins 3
rs587782717
BRCA2
0.925 0.200 13 32340445 frameshift variant -/A delins 3
rs63750149
MSH2
1.000 0.160 2 47478395 frameshift variant -/A delins 3