ClinVar Miner

Submissions for variant NM_001378964.1(CDON):c.349+14T>C

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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 RCV003640602 SCV004467421 likely benign Holoprosencephaly 11 2023-06-03 criteria provided, single submitter clinical testing

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