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: 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: rs397507838
rs397507838
BRCA2
1 1.000 0.080 13 32340636 missense variant A/C;G snv 8.2E-06 7.0E-06 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: rs41293447
rs41293447
BRCA1
1 1.000 0.080 17 43092229 missense variant C/T snv 1.2E-04 6.2E-04 0.700 1.000 20 1994 2017
dbSNP: rs55688530
rs55688530
BRCA1
1 1.000 0.080 17 43097280 missense variant G/A;T snv 6.9E-04 0.700 1.000 20 1994 2017
dbSNP: rs55712212
rs55712212
BRCA2
1 1.000 0.080 13 32341176 missense variant G/A;T snv 1.5E-03 1.2E-03 0.700 1.000 20 1997 2006
dbSNP: rs55716624
rs55716624
BRCA2
1 1.000 0.080 13 32356496 missense variant C/A;T snv 2.7E-04 9.8E-04 0.700 1.000 20 1997 2006
dbSNP: rs55815649
rs55815649
BRCA1
1 1.000 0.080 17 43074406 missense variant C/T snv 3.9E-04 1.4E-03 0.700 1.000 20 1994 2017
dbSNP: rs56046357
rs56046357
BRCA1
1 1.000 0.080 17 43094148 missense variant A/T snv 7.0E-06 0.700 1.000 20 1994 2017
dbSNP: rs56195342
rs56195342
BRCA1
1 1.000 0.080 17 43063368 missense variant T/C snv 1.8E-04 1.1E-04 0.700 1.000 20 1994 2017
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: rs56214134
rs56214134
BRCA1
2 0.925 0.080 17 43091931 missense variant C/A;G snv 1.2E-04; 2.3E-04 0.700 1.000 20 1994 2017
dbSNP: rs587780646
rs587780646
BRCA2
1 1.000 0.080 13 32333316 missense variant T/G snv 7.0E-05 2.8E-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: rs769650474
rs769650474
BRCA1
1 1.000 0.080 17 43115727 missense variant T/G snv 1.2E-05 1.4E-05 0.700 1.000 20 1994 2017
dbSNP: rs786202389
rs786202389
BRCA1
1 1.000 0.080 17 43057091 missense variant G/C snv 0.700 1.000 20 1994 2017
dbSNP: rs786203152
rs786203152
BRCA1 ; NBR2
1 1.000 0.080 17 43124086 missense variant G/A snv 0.700 1.000 20 1994 2017
dbSNP: rs79538375
rs79538375
BRCA2
1 1.000 0.080 13 32340140 missense variant A/G snv 8.9E-04 3.1E-04 0.700 1.000 20 1997 2006
dbSNP: rs80356865
rs80356865
BRCA1
1 1.000 0.080 17 43094797 missense variant T/A snv 1.2E-05 0.700 1.000 20 1994 2017
dbSNP: rs80356929
rs80356929
BRCA1 ; NBR2
3 0.925 0.080 17 43124044 missense variant A/C;G;T snv 0.700 1.000 20 1994 2017
dbSNP: rs80357078
rs80357078
BRCA1
2 1.000 0.080 17 43049162 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 20 1994 2017
dbSNP: rs80357094
rs80357094
BRCA1
2 0.925 0.080 17 43063881 missense variant G/C;T snv 0.700 1.000 20 1994 2017