ClinVar Miner

Submissions for variant NM_025099.6(CTC1):c.3012-5_3012-2del

dbSNP: rs2151500920
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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 RCV002090903 SCV002379091 likely benign Dyskeratosis congenita 2021-06-01 criteria provided, single submitter clinical testing

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