Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80358920
BRCA2
0.732 0.400 13 32346841 stop gained C/G;T snv 14
rs80359212
BRCA2
0.763 0.320 13 32394814 stop gained C/T snv 1.2E-05 4.2E-05 11
rs80358427
BRCA2
0.776 0.280 13 32332877 stop gained A/T snv 4.0E-06 10
rs80358785
BRCA2
0.790 0.240 13 32340000 stop gained C/A;G snv 1.6E-05 9
rs80359550
BRCA2
0.807 0.280 13 32340301 frameshift variant T/- del 1.8E-04 8
rs80359584
BRCA2
0.807 0.280 13 32340757 frameshift variant CTTAA/- delins 4.2E-06 1.4E-05 8
rs80358981
BRCA2
0.827 0.200 13 32356550 stop gained C/T snv 2.0E-05 1.4E-05 7
rs80359351
BRCA2
0.851 0.200 13 32337161 frameshift variant ACAA/- delins 2.1E-05 6
rs397507828
BRCA2
1.000 13 32340440 stop gained G/T snv 4
rs587782780
BRCA2
0.925 0.200 13 32336414 frameshift variant GATTA/- del 4.0E-06 4
rs80358529
BRCA2
0.925 0.200 13 32319283 stop gained C/T snv 4
rs80359759
BRCA2
0.925 0.200 13 32394832 frameshift variant G/- delins 4
rs81002796
BRCA2
0.925 0.200 13 32316528 splice donor variant G/A;C;T snv 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
rs878853559
BRCA2
0.925 0.200 13 32336450 stop gained C/T snv 4
rs879255309
BRCA2
0.925 0.200 13 32338238 stop gained C/T snv 4
rs1057518637
BRCA2
1.000 13 32336621 stop gained C/G;T snv 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
rs771203198
BRCA2
0.925 0.200 13 32394750 stop gained G/A;C snv 4.0E-06 3
rs80359222
BRCA2
0.925 0.200 13 32394913 stop gained A/G;T snv 3
rs80359706
BRCA2
1.000 13 32363522 frameshift variant -/T delins 3