ClinVar Miner

Submissions for variant NM_018718.3(CEP41):c.33+20C>A

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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 RCV002867949 SCV003240337 likely benign Joubert syndrome 15 2022-10-07 criteria provided, single submitter clinical testing

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