ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.6334A>T (p.Arg2112Ter)

dbSNP: rs2137526529
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine, Sinai Health System RCV001357973 SCV001553588 uncertain significance not provided no assertion criteria provided clinical testing

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