ClinVar Miner

Submissions for variant NM_003504.5(CDC45):c.1559+18G>A

dbSNP: rs13447282
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 RCV001545020 SCV001764265 likely benign not provided 2019-11-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001545020 SCV002401104 benign not provided 2025-01-29 criteria provided, single submitter clinical testing

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