ClinVar Miner

Submissions for variant NM_018451.5(CENPJ):c.2992-6del

dbSNP: rs35599563
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 RCV001548419 SCV001768326 likely benign not provided 2019-09-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001548419 SCV004394636 benign not provided 2023-03-17 criteria provided, single submitter clinical testing

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