ClinVar Miner

Submissions for variant NM_152383.5(DIS3L2):c.703-3del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003644396 SCV004464224 benign Perlman syndrome 2023-05-08 criteria provided, single submitter clinical testing

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