ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.8576A>G (p.Gln2859Arg)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003322533 SCV004027483 uncertain significance not specified 2023-08-15 criteria provided, single submitter clinical testing
Baylor Genetics RCV004572926 SCV005059029 uncertain significance Familial cancer of breast 2024-02-26 criteria provided, single submitter clinical testing

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