ClinVar Miner

Submissions for variant NM_025099.6(CTC1):c.1819-19A>C

dbSNP: rs2507908587
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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 RCV003529844 SCV004329301 likely benign Dyskeratosis congenita 2023-10-23 criteria provided, single submitter clinical testing

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