ClinVar Miner

Submissions for variant NM_001080449.3(DNA2):c.2697+18del

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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 RCV002863120 SCV003229772 likely benign not provided 2022-10-31 criteria provided, single submitter clinical testing

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