ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4064dup (p.Asn1355fs)

dbSNP: rs2053475644
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001252984 SCV001428472 pathogenic Breast-ovarian cancer, familial, susceptibility to, 1 2019-01-09 criteria provided, single submitter clinical testing

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