ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.1034A>G (p.Lys345Arg) (rs1555281704)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000567450 SCV000668748 uncertain significance Hereditary cancer-predisposing syndrome 2017-01-26 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000508268 SCV000600459 uncertain significance not specified 2017-05-09 criteria provided, single submitter clinical testing

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