ClinVar Miner

Submissions for variant NM_018718.3(CEP41):c.30T>G (p.Pro10=)

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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 RCV003852840 SCV004652926 likely benign Joubert syndrome 15 2023-10-22 criteria provided, single submitter clinical testing

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