ClinVar Miner

Submissions for variant NM_018718.3(CEP41):c.186A>G (p.Lys62=)

gnomAD frequency: 0.00001  dbSNP: rs1797202624
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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 RCV001456638 SCV001660424 likely benign Joubert syndrome 15 2022-08-09 criteria provided, single submitter clinical testing

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