rs1800751
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway.
|
29339979 |
2018 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium.
|
28490613 |
2018 |
rs55851803
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Genetic and clinical characteristics in Japanese hereditary breast and ovarian cancer: first report after establishment of HBOC registration system in Japan.
|
29176636 |
2018 |
rs80356898
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
BRCA1 and BRCA2 germline variants in breast cancer patients from the Republic of Macedonia.
|
29335924 |
2018 |
rs80356936
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Mutations in context: implications of BRCA testing in diverse populations.
|
28918466 |
2018 |
rs80357115
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
The yield of targeted genotyping for the recurring mutations in BRCA1/2 in Israel.
|
29086229 |
2018 |
rs80357389
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway.
|
29339979 |
2018 |
rs80357389
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs80357472
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Genetic and clinical characteristics in Japanese hereditary breast and ovarian cancer: first report after establishment of HBOC registration system in Japan.
|
29176636 |
2018 |
rs80357472
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs80357472
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Germline BRCA mutation and outcome in young-onset breast cancer (POSH): a prospective cohort study.
|
29337092 |
2018 |
rs80357762
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs80357808
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Characterization of mutations in BRCA1/2 and the relationship with clinic-pathological features of breast cancer in a hereditarily high-risk sample of chinese population.
|
29435039 |
2018 |
rs80357877
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Is there a genetic anticipation in breast and/or ovarian cancer families with the germline c.3481_3491del11 mutation?
|
28493033 |
2018 |
rs80358099
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Gene-panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication.
|
28802053 |
2018 |
rs80358145
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs876659327
|
|
TC |
0.700 |
CausalMutation |
CLINVAR |
High prevalence of deleterious BRCA1 and BRCA2 germline mutations in arab breast and ovarian cancer patients.
|
29297111 |
2018 |
rs1800751
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Characterization of BRCA1 and BRCA2 variants found in a Norwegian breast or ovarian cancer cohort.
|
27495310 |
2017 |
rs28897672
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Multiple-gene panel analysis in a case series of 255 women with hereditary breast and ovarian cancer.
|
28423363 |
2017 |
rs28897672
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.
|
28324225 |
2017 |
rs28897672
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Molecular characterization and clinical interpretation of BRCA1/BRCA2 variants in families from Murcia (south-eastern Spain) with hereditary breast and ovarian cancer: clinical-pathological features in BRCA carriers and non-carriers.
|
28477318 |
2017 |
rs28897686
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas.
|
27767231 |
2017 |
rs28897696
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Molecular characterization and clinical interpretation of BRCA1/BRCA2 variants in families from Murcia (south-eastern Spain) with hereditary breast and ovarian cancer: clinical-pathological features in BRCA carriers and non-carriers.
|
28477318 |
2017 |
rs387906563
|
|
GCCACATGGCT |
0.700 |
CausalMutation |
CLINVAR |
Mutations in BRCA1, BRCA2 and other breast and ovarian cancer susceptibility genes in Central and South American populations.
|
28985766 |
2017 |
rs397509284
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients.
|
28724667 |
2017 |