ClinVar Miner

Submissions for variant NM_004448.3(ERBB2):c.2313_2324dup (p.Tyr772_Ala775dup) (rs397516975)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000038123 SCV000061789 likely pathogenic Non-small cell lung cancer 2012-05-15 criteria provided, single submitter clinical testing
OMIM RCV000014889 SCV000035144 pathogenic Lung adenocarcinoma 2004-09-30 no assertion criteria provided literature only

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