ClinVar Miner

Submissions for variant NM_007294.3(BRCA1):c.4987-68A>G (rs8176234)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breast Cancer Information Core (BIC) (BRCA1) RCV000112451 SCV000145247 not provided Breast-ovarian cancer, familial 1 no assertion provided clinical testing
Breast Cancer Information Core (BIC) (BRCA1) RCV000112451 SCV000145248 benign Breast-ovarian cancer, familial 1 2002-05-29 no assertion criteria provided clinical testing
Color RCV000580916 SCV000683234 benign Hereditary cancer-predisposing syndrome 2014-12-11 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000502724 SCV000591556 benign not specified criteria provided, single submitter clinical testing
Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) RCV000112451 SCV000244643 benign Breast-ovarian cancer, familial 1 2015-01-12 reviewed by expert panel curation Class 1 not pathogenic based on frequency >1% in an outbred sampleset. Frequency 0.3322 (Asian), 0.2175 (African), 0.3615 (European), derived from 1000 genomes (2012-04-30).
Genome Diagnostics Laboratory,University Medical Center Utrecht RCV000112451 SCV000743383 benign Breast-ovarian cancer, familial 1 2014-10-09 criteria provided, single submitter clinical testing

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