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: rs273900729
rs273900729
BRCA1
2 0.925 0.160 17 43082529 missense variant A/G snv 0.700 0
dbSNP: rs28897701
rs28897701
BRCA2
2 0.925 0.160 13 32319232 missense variant G/C snv 2.6E-04 3.1E-04 0.700 0
dbSNP: rs34612342
rs34612342
MUTYH
32 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.700 0
dbSNP: rs35394823
rs35394823
DPH1 ; OVCA2
1 1.000 0.120 17 2040586 missense variant C/G snv 8.1E-02 6.8E-02 0.700 0
dbSNP: rs372000848
rs372000848
MRE11
1 1.000 0.120 11 94470575 missense variant G/A snv 5.2E-05 7.7E-05 0.700 0
dbSNP: rs41293521
rs41293521
BRCA2
2 0.925 0.160 13 32394724 missense variant T/C snv 2.9E-04 2.5E-04 0.700 0
dbSNP: rs4987046
rs4987046
BRCA2
4 0.925 0.160 13 32319134 missense variant A/G snv 1.6E-03 1.6E-03 0.700 0
dbSNP: rs56070345
rs56070345
BRCA2
1 1.000 0.120 13 32356497 missense variant G/A;C;T snv 6.4E-05 0.700 0
dbSNP: rs587776650
rs587776650
NBN
11 0.790 0.280 8 89971214 frameshift variant GTTTT/- delins 2.0E-04 0.700 0
dbSNP: rs587781803
rs587781803
BRCA2
5 0.851 0.200 13 32341169 frameshift variant AAGAG/- delins 0.700 0
dbSNP: rs63750695
rs63750695
PMS2
6 0.851 0.280 7 5978675 frameshift variant AAGTT/- delins 0.700 0
dbSNP: rs778705666
rs778705666
DPH1
1 1.000 0.120 17 2030174 missense variant C/T snv 0.700 0
dbSNP: rs80187739
rs80187739
BRCA1
5 0.851 0.200 17 43067608 missense variant C/A;G;T snv 1.2E-05 0.700 0
dbSNP: rs80356898
rs80356898
BRCA1
11 0.752 0.200 17 43093844 stop gained G/A;C snv 2.8E-05; 4.0E-06 0.700 0
dbSNP: rs80356993
rs80356993
BRCA1
3 0.925 0.120 17 43063937 missense variant A/G;T snv 0.700 0
dbSNP: rs80357233
rs80357233
BRCA1
4 0.882 0.200 17 43093393 stop gained G/C;T snv 4.0E-06 0.700 0
dbSNP: rs80357438
rs80357438
BRCA1 ; NBR2
5 0.851 0.200 17 43124032 stop gained A/G;T snv 0.700 0
dbSNP: rs80357462
rs80357462
BRCA1
1 1.000 0.120 17 43057083 missense variant G/A;C snv 0.700 0
dbSNP: rs80357474
rs80357474
BRCA1
5 0.827 0.200 17 43049188 missense variant A/C;G;T snv 8.0E-06 0.700 0
dbSNP: rs80357669
rs80357669
BRCA1
5 0.851 0.200 17 43093074 frameshift variant G/- delins 0.700 0
dbSNP: rs80357828
rs80357828
BRCA1
3 0.882 0.200 17 43092155 frameshift variant GA/- delins 0.700 0
dbSNP: rs80358479
rs80358479
BRCA2
1 1.000 0.120 13 32333367 missense variant C/T snv 2.1E-04 1.2E-04 0.700 0
dbSNP: rs80358981
rs80358981
BRCA2
7 0.827 0.200 13 32356550 stop gained C/T snv 2.0E-05 1.4E-05 0.700 0
dbSNP: rs80359078
rs80359078
BRCA2
3 0.882 0.160 13 32370430 missense variant G/A snv 3.2E-05 2.1E-05 0.700 0
dbSNP: rs80359176
rs80359176
BRCA2
1 1.000 0.120 13 32380076 missense variant C/T snv 3.6E-05 7.0E-06 0.700 0