ClinVar Miner

Submissions for variant NM_003672.4(CDC14A):c.520-16T>C

gnomAD frequency: 0.00928  dbSNP: rs28364872
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001559599 SCV001781863 likely benign not provided 2018-07-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001559599 SCV002493844 benign not provided 2024-01-13 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001559599 SCV005259176 likely benign not provided criteria provided, single submitter not provided

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