ClinVar Miner

Submissions for variant NM_001099274.3(TINF2):c.1185C>T (p.Asp395=)

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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 RCV002606592 SCV003505141 likely benign Dyskeratosis congenita 2022-06-02 criteria provided, single submitter clinical testing

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