ClinVar Miner

Submissions for variant NM_001378609.3(OTOGL):c.5729C>T (p.Thr1910Met)

dbSNP: rs375155261
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001551102 SCV001771533 uncertain significance not provided 2020-08-17 criteria provided, single submitter clinical testing In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Labcorp Genetics (formerly Invitae), Labcorp RCV001551102 SCV002406205 benign not provided 2024-08-04 criteria provided, single submitter clinical testing

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