ClinVar Miner

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

dbSNP: rs35902828
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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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

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