ClinVar Miner

Submissions for variant NM_001174150.2(ARL13B):c.1210+14A>G

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002619208 SCV003497477 likely benign Joubert syndrome 8 2024-12-05 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002619208 SCV005659796 uncertain significance Joubert syndrome 8 2024-04-25 criteria provided, single submitter clinical testing

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