ClinVar Miner

Submissions for variant NM_004153.4(ORC1):c.1239A>C (p.Ala413=)

gnomAD frequency: 0.00019  dbSNP: rs377164890
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
Genetic Services Laboratory, University of Chicago RCV000117872 SCV000152144 benign not specified 2013-12-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000877478 SCV001020219 likely benign not provided 2025-01-01 criteria provided, single submitter clinical testing

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