ClinVar Miner

Submissions for variant NM_001379200.1(TBX1):c.437+18C>G

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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 RCV003095794 SCV003486114 likely benign DiGeorge syndrome 2022-05-18 criteria provided, single submitter clinical testing

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