ClinVar Miner

Submissions for variant NM_001379200.1(TBX1):c.1131G>C (p.Val377=)

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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 RCV005185782 SCV005822873 likely benign DiGeorge syndrome 2024-12-18 criteria provided, single submitter clinical testing

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