Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs144848
BRCA2
0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs11571818
BRCA2
0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 17
rs41293497
BRCA2
0.724 0.440 13 32340037 stop gained C/A;G;T snv 4.0E-06; 2.0E-05 14
rs80358807
BRCA2
0.763 0.280 13 32340146 stop gained C/T snv 10
rs28897743
BRCA2
0.827 0.280 13 32346896 missense variant G/A;C;T snv 4.0E-06 8
rs11571707
BRCA2
0.851 0.200 13 32356461 missense variant T/C snv 1.9E-02 8.5E-03 7
rs397507758
BRCA2
0.807 0.200 13 32339456 stop gained C/T snv 6
rs80358829
BRCA2
0.827 0.120 13 32340327 missense variant C/T snv 6
rs80359306
BRCA2
0.827 0.280 13 32333284 frameshift variant A/-;AA delins 6
rs1799944
BRCA2
0.882 0.080 13 32337326 missense variant A/G snv 5.4E-02 4.5E-02 5
rs28897759
BRCA2
0.851 0.200 13 32394803 missense variant A/G;T snv 4.0E-06; 4.0E-06 5
rs41293477
BRCA2
0.851 0.200 13 32337513 stop gained T/G snv 7.0E-06 5
rs80358547
BRCA2
0.851 0.200 13 32316462 start lost T/A;C;G snv 8.0E-06 5
rs80358561
BRCA2
0.851 0.200 13 32319323 stop gained T/G snv 5
rs80359065
BRCA2
0.827 0.240 13 32363389 missense variant G/A;T snv 7.9E-04 5
rs80359130
BRCA2
0.827 0.200 13 32376769 missense variant C/A;G;T snv 8.0E-06 5
rs80359152
BRCA2
0.851 0.200 13 32379800 missense variant G/A snv 5
rs80359770
BRCA2
0.851 0.200 13 32332429 frameshift variant A/-;AA delins 5
rs483353122
BRCA2
0.851 0.200 13 32363410 frameshift variant -/AG ins 4
rs4987117
BRCA2
0.925 0.080 13 32340099 missense variant C/T snv 1.8E-02 1.8E-02 4
rs765436962
BRCA2
0.851 0.120 13 32332790 missense variant G/T snv 1.6E-05 4
rs80358702
BRCA2
0.882 0.080 13 32326150 missense variant G/A;C snv 4
rs80358732
BRCA2
0.925 0.080 13 32339451 missense variant A/G snv 2.2E-05 2.1E-05 4
rs80359011
BRCA2
0.882 0.200 13 32362574 stop gained G/A;C snv 4