ClinVar Miner

Submissions for variant NM_014264.5(PLK4):c.1830+7C>G

gnomAD frequency: 0.00061  dbSNP: rs367752526
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000963437 SCV001110591 benign not provided 2024-01-18 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001819051 SCV002069401 uncertain significance not specified 2018-07-19 criteria provided, single submitter clinical testing

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