Gene: BRCA2 ×
Source: BEFREE ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs28897759
rs28897759
BRCA2
2 0.851 0.200 13 32394803 missense variant A/G;T snv 4.0E-06; 4.0E-06 0.810 1.000 1 2014 2014
dbSNP: rs11571833
rs11571833
BRCA2
31 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 0.740 0.800 4 2013 2016
dbSNP: rs80359065
rs80359065
BRCA2
5 0.827 0.240 13 32363389 missense variant G/A;T snv 7.9E-04 0.730 1.000 3 2003 2017
dbSNP: rs28897743
rs28897743
BRCA2
4 0.827 0.280 13 32346896 missense variant G/A;C;T snv 4.0E-06 0.710 1.000 1 2020 2020
dbSNP: rs80358755
rs80358755
BRCA2
2 0.925 0.080 13 32339667 missense variant G/A;T snv 3.4E-04; 4.0E-06 0.710 1.000 1 1997 2016
dbSNP: rs80358807
rs80358807
BRCA2
2 0.763 0.280 13 32340146 stop gained C/T snv 0.710 1.000 1 2017 2017
dbSNP: rs80359078
rs80359078
BRCA2
2 0.882 0.160 13 32370430 missense variant G/A snv 3.2E-05 2.1E-05 0.710 1.000 1 2016 2016
dbSNP: rs80359182
rs80359182
BRCA2
2 0.925 0.080 13 32319100 missense variant T/C;G snv 0.710 1.000 1 2019 2019
dbSNP: rs80359198
rs80359198
BRCA2
1 0.882 0.200 13 32394717 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 7.6E-05 0.710 1.000 1 1996 1996
dbSNP: rs144848
rs144848
BRCA2
29 0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 0.100 0.923 13 2000 2017
dbSNP: rs11571653
rs11571653
BRCA2
2 0.925 0.080 13 32336705 missense variant A/G snv 2.3E-04 1.7E-04 0.030 1.000 3 2003 2017
dbSNP: rs4987117
rs4987117
BRCA2
4 0.925 0.080 13 32340099 missense variant C/T snv 1.8E-02 1.8E-02 0.030 1.000 3 2005 2019
dbSNP: rs80358527
rs80358527
BRCA2
2 0.925 0.080 13 32316486 missense variant C/A;G;T snv 8.0E-06 0.020 0.500 2 2006 2009
dbSNP: rs80358829
rs80358829
BRCA2
6 0.827 0.120 13 32340327 missense variant C/T snv 0.020 1.000 2 2005 2015
dbSNP: rs80358978
rs80358978
BRCA2
2 0.925 0.080 13 32356514 missense variant G/A snv 1.6E-04 3.5E-05 0.020 1.000 2 2017 2017
dbSNP: rs876659602
rs876659602
BRCA2
3 0.882 0.080 13 32337468 missense variant A/G snv 0.020 1.000 2 2013 2016
dbSNP: rs1057520611
rs1057520611
BRCA2
2 0.925 0.080 13 32356462 missense variant A/G snv 0.010 1.000 1 2006 2006
dbSNP: rs11571707
rs11571707
BRCA2
7 0.851 0.200 13 32356461 missense variant T/C snv 1.9E-02 8.5E-03 0.010 < 0.001 1 2010 2010
dbSNP: rs1334767632
rs1334767632
BRCA2
2 0.925 0.080 13 32332437 missense variant T/C snv 7.0E-06 0.010 1.000 1 2020 2020
dbSNP: rs15869
rs15869
BRCA2
3 0.925 0.080 13 32398875 3 prime UTR variant A/C snv 0.15 0.010 1.000 1 2016 2016
dbSNP: rs1799944
rs1799944
BRCA2
5 0.882 0.080 13 32337326 missense variant A/G snv 5.4E-02 4.5E-02 0.010 1.000 1 2009 2009
dbSNP: rs1799955
rs1799955
BRCA2
2 0.925 0.080 13 32355095 synonymous variant A/G;T snv 0.23; 8.0E-06 0.010 < 0.001 1 2009 2009
dbSNP: rs1801426
rs1801426
BRCA2
3 0.882 0.120 13 32398747 missense variant A/G snv 2.3E-02 3.8E-02 0.010 < 0.001 1 2017 2017
dbSNP: rs1801439
rs1801439
BRCA2
2 0.925 0.080 13 32332843 synonymous variant A/G snv 5.2E-02 3.8E-02 0.010 < 0.001 1 2009 2009
dbSNP: rs206340
rs206340
BRCA2
2 0.925 0.080 13 32391173 intron variant G/A snv 0.21 0.010 1.000 1 2004 2004