ClinVar Miner

Submissions for variant NM_001378609.3(OTOGL):c.6616-19C>T

gnomAD frequency: 0.00025  dbSNP: rs144322810
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001568592 SCV001792495 likely benign not provided 2018-11-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001568592 SCV002331877 benign not provided 2023-12-14 criteria provided, single submitter clinical testing

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