Gene: BRCA2 ×
Source: ALL
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: rs397507595
rs397507595
BRCA2
1 1.000 0.080 13 32319167 missense variant A/G snv 0.700 1.000 25 1997 2014
dbSNP: rs397507674
rs397507674
BRCA2
1 1.000 0.080 13 32337891 missense variant G/A snv 4.0E-06 0.700 1.000 25 1997 2014
dbSNP: rs397507770
rs397507770
BRCA2
1 1.000 0.080 13 32339543 missense variant A/T snv 8.2E-06 0.700 1.000 25 1997 2014
dbSNP: rs397507822
rs397507822
BRCA2
1 1.000 0.080 13 32326584 missense variant C/G;T snv 0.700 1.000 25 1997 2014
dbSNP: rs397507847
rs397507847
BRCA2
1 1.000 0.080 13 32340739 missense variant A/C;G snv 0.700 1.000 25 1997 2014
dbSNP: rs397507873
rs397507873
BRCA2
1 1.000 0.080 13 32329475 missense variant C/T snv 0.700 1.000 25 1997 2014
dbSNP: rs397507912
rs397507912
BRCA2
4 0.882 0.200 13 32355219 stop gained C/G;T snv 0.700 1.000 25 1997 2014
dbSNP: rs45580035
rs45580035
BRCA2
8 0.790 0.240 13 32380043 missense variant C/T snv 1.2E-05 0.800 1.000 25 1997 2014
dbSNP: rs80358507
rs80358507
BRCA2
1 1.000 0.080 13 32319250 missense variant T/A;C;G snv 2.4E-05; 8.0E-06 0.700 1.000 25 1997 2014
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 21 1997 2016
dbSNP: rs28897716
rs28897716
BRCA2
1 1.000 0.080 13 32337158 missense variant G/A;C;T snv 6.1E-04; 6.4E-05 0.700 1.000 20 1997 2006
dbSNP: rs28897749
rs28897749
BRCA2
3 0.882 0.120 13 32363384 missense variant G/A;C snv 2.1E-03; 4.0E-06 0.700 1.000 20 1997 2006
dbSNP: rs397507615
rs397507615
BRCA2
1 1.000 0.080 13 32319200 missense variant C/T snv 4.0E-06 0.700 1.000 20 1997 2006
dbSNP: rs397507620
rs397507620
BRCA2
1 1.000 0.080 13 32336542 missense variant A/G snv 0.700 1.000 20 1997 2006
dbSNP: rs397507795
rs397507795
BRCA2
1 1.000 0.080 13 32340015 missense variant C/G;T snv 2.4E-05 0.700 1.000 20 1997 2006
dbSNP: rs397507875
rs397507875
BRCA2
1 1.000 0.080 13 32341020 missense variant A/G snv 1.6E-05 0.700 1.000 20 1997 2006
dbSNP: rs397508057
rs397508057
BRCA2
1 1.000 0.080 13 32319103 missense variant T/C snv 0.700 1.000 20 1997 2006
dbSNP: rs398122784
rs398122784
BRCA2
1 1.000 0.080 13 32339094 missense variant G/A snv 0.700 1.000 20 1997 2006
dbSNP: rs56204128
rs56204128
BRCA2
1 1.000 0.080 13 32394785 missense variant T/C;G snv 1.6E-05 0.700 1.000 20 1997 2006
dbSNP: rs757577670
rs757577670
BRCA2
1 1.000 0.080 13 32336538 missense variant A/C;T snv 4.0E-06 0.700 1.000 20 1997 2006
dbSNP: rs80358388
rs80358388
BRCA2
1 1.000 0.080 13 32398583 missense variant C/G;T snv 4.0E-06 0.700 1.000 20 1997 2006
dbSNP: rs80358600
rs80358600
BRCA2
3 0.882 0.200 13 32337870 stop gained C/A;G;T snv 1.4E-03 0.700 1.000 20 1997 2006
dbSNP: rs80358862
rs80358862
BRCA2
1 1.000 0.080 13 32340570 missense variant C/A;G;T snv 8.0E-06; 1.6E-05 0.700 1.000 20 1997 2006
dbSNP: rs80358876
rs80358876
BRCA2
1 1.000 0.080 13 32340758 missense variant A/C;T snv 4.2E-06; 4.2E-06 0.700 1.000 20 1997 2006
dbSNP: rs80358912
rs80358912
BRCA2
1 1.000 0.080 13 32344593 missense variant T/C snv 6.8E-05 0.700 1.000 20 1997 2006