ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.1811A>G (p.Tyr604Cys)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, Skane University Hospital Lund RCV004697422 SCV005196768 uncertain significance not provided 2022-05-27 criteria provided, single submitter clinical testing

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