ClinVar Miner

Submissions for variant NM_016343.4(CENPF):c.6550G>A (p.Val2184Ile)

gnomAD frequency: 0.00435  dbSNP: rs62623663
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000961920 SCV001108976 benign not provided 2024-11-28 criteria provided, single submitter clinical testing
GeneDx RCV000961920 SCV001795422 likely benign not provided 2020-03-12 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001819036 SCV002068451 benign not specified 2018-03-01 criteria provided, single submitter clinical testing

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