ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.10529-303del

dbSNP: rs71287326
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001688946 SCV001915637 benign not provided 2019-11-29 criteria provided, single submitter clinical testing

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