ClinVar Miner

Submissions for variant NM_006265.3(RAD21):c.815-27dup

dbSNP: rs35902828
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001571188 SCV001795609 likely benign not provided 2019-08-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002488392 SCV002798981 likely benign Mungan syndrome; Cornelia de Lange syndrome 4 2022-05-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005094806 SCV005821859 benign Cornelia de Lange syndrome 4 2024-12-11 criteria provided, single submitter clinical testing

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