ClinVar Miner

Submissions for variant NM_001363.5(DKC1):c.1383A>G (p.Ala461=)

dbSNP: rs1293654532
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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 RCV002108322 SCV002434246 likely benign Dyskeratosis congenita 2023-12-31 criteria provided, single submitter clinical testing

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