ClinVar Miner

Submissions for variant NM_006265.3(RAD21):c.1162-6del

dbSNP: rs369816312
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
Genetic Services Laboratory, University of Chicago RCV000193001 SCV000248643 benign not specified 2013-09-26 criteria provided, single submitter clinical testing
GeneDx RCV001636716 SCV001851663 benign not provided 2019-08-08 criteria provided, single submitter clinical testing

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