ClinVar Miner

Submissions for variant NM_001363.5(DKC1):c.1233C>T (p.Thr411=)

dbSNP: rs2071872349
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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 RCV003647222 SCV004553841 likely benign Dyskeratosis congenita 2024-01-14 criteria provided, single submitter clinical testing

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