ClinVar Miner

Submissions for variant NM_032043.2(BRIP1):c.2472C>T (p.Ala824=) (rs767666616)

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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 RCV000574587 SCV000661583 likely benign Hereditary cancer-predisposing syndrome 2017-02-14 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759710 SCV000889215 uncertain significance not provided 2017-12-27 criteria provided, single submitter clinical testing

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