ClinVar Miner

Submissions for variant NM_018486.3(HDAC8):c.738-4A>G

dbSNP: rs782294776
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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 RCV002200885 SCV002488832 likely benign Cornelia de Lange syndrome 5 2022-06-07 criteria provided, single submitter clinical testing

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