ClinVar Miner

Submissions for variant NM_006265.3(RAD21):c.274+26GTT[5]

dbSNP: rs112562183
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001663217 SCV001872590 benign not provided 2019-08-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001796659 SCV002033416 benign Mungan syndrome 2021-11-07 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001796658 SCV002033418 benign Cornelia de Lange syndrome 4 2021-11-07 criteria provided, single submitter clinical testing

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