ClinVar Miner

Submissions for variant NM_001292063.2(OTOG):c.15G>A (p.Ala5=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002467129 SCV002762203 uncertain significance not provided 2022-06-06 criteria provided, single submitter clinical testing In silico analysis supports that this variant does not alter splicing; Has not been previously published as pathogenic or benign to our knowledge
Labcorp Genetics (formerly Invitae), Labcorp RCV002467129 SCV005691508 likely benign not provided 2024-07-30 criteria provided, single submitter clinical testing

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