ClinVar Miner

Submissions for variant NM_001099274.3(TINF2):c.9G>A (p.Thr3=)

dbSNP: rs748683638
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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 RCV002166661 SCV002473453 likely benign Dyskeratosis congenita 2020-12-27 criteria provided, single submitter clinical testing

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