ClinVar Miner

Submissions for variant NM_004526.4(MCM2):c.2604+17G>A

gnomAD frequency: 0.00001  dbSNP: rs3813266
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002140159 SCV002455826 likely benign not provided 2023-03-04 criteria provided, single submitter clinical testing

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