Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518636
BRCA1
1.000 17 43047646 frameshift variant -/A ins 3
rs276174819
BRCA2
0.925 0.200 13 32336524 frameshift variant -/A delins 3
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs886037798
BRCA2
1.000 13 32340886 frameshift variant -/C delins 2
rs80357906
BRCA1
0.827 0.200 17 43057062 frameshift variant -/G delins 1.8E-04 8
rs1555281594
BRCA2
1.000 13 32332276 frameshift variant -/G delins 2
rs886037786
BRCA1
1.000 17 43094231 frameshift variant -/G delins 2
rs397508979
BRCA1
17 43092974 frameshift variant -/GAAAAGTGAA ins 1
rs1057519737
MIR4728 ; ERBB2
17 39724750 inframe insertion -/GCTCCCCAG delins 1
rs1555526250
TP53
17 7675191 frameshift variant -/GGTCT delins 1
rs80357783
NBR2 ; BRCA1
0.851 0.200 17 43124030 frameshift variant -/T delins 4.0E-06 6
rs80357714
BRCA1
0.925 0.200 17 43094150 frameshift variant -/T delins 4
rs80359706
BRCA2
1.000 13 32363522 frameshift variant -/T delins 3
rs886037788
BRCA1
17 43091461 frameshift variant -/TCAA ins 1
rs397516979
ERBB2 ; MIR4728
1.000 0.080 17 39724744 protein altering variant -/TCT;TGT;TTT ins 2
rs864622401
BRCA2
0.882 0.200 13 32339092 frameshift variant -/TG delins 4
rs121913289
PTEN
1.000 0.080 10 87958013 frameshift variant A/- delins 4
rs483353111
BRCA2
0.925 0.200 13 32336949 frameshift variant A/- delins 3
rs1057517590
BRCA1
1.000 17 43063370 frameshift variant A/- del 2
rs886037784
BRCA1
1.000 17 43099803 frameshift variant A/- del 2
rs886037790
BRCA1
1.000 17 43071202 frameshift variant A/- delins 2
rs886037804
BRCA2
1.000 13 32379805 frameshift variant A/- delins 2
rs886040109
BRCA1
1.000 17 43092265 frameshift variant A/- delins 2
rs1057519939
PIK3CA
0.776 0.160 3 179203763 missense variant A/C snv 10
rs1057519987
TP53
0.776 0.280 17 7673810 missense variant A/C snv 10