ClinVar Miner

Submissions for variant NM_152274.5(CCNQ):c.501C>T (p.Ala167=)

gnomAD frequency: 0.00004  dbSNP: rs782615471
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001730239 SCV003477282 benign not provided 2023-04-06 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001730239 SCV001978066 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001730239 SCV001980623 likely benign not provided no assertion criteria provided clinical testing

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