ClinVar Miner

Submissions for variant NM_020964.3(EPG5):c.1944-16C>T

dbSNP: rs575676819
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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 RCV001514866 SCV001722819 benign Vici syndrome 2023-12-24 criteria provided, single submitter clinical testing

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