ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.-21_672+21del

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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 RCV004697588 SCV005197842 pathogenic not provided 2022-05-27 criteria provided, single submitter clinical testing

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