ClinVar Miner

Submissions for variant NM_005996.4(TBX3):c.1272C>T (p.Ser424=)

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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 RCV005184272 SCV005814770 likely benign Ulnar-mammary syndrome 2024-04-02 criteria provided, single submitter clinical testing

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