ClinVar Miner

Submissions for variant NM_025099.6(CTC1):c.2013C>G (p.Ser671=)

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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 RCV003116616 SCV003792823 likely benign Dyskeratosis congenita 2022-07-15 criteria provided, single submitter clinical testing

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