ClinVar Miner

Submissions for variant NM_025099.6(CTC1):c.1638C>T (p.Pro546=)

dbSNP: rs2151517678
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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 RCV001459666 SCV001663515 likely benign Dyskeratosis congenita 2024-09-03 criteria provided, single submitter clinical testing

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