ClinVar Miner

Submissions for variant NM_001378609.3(OTOGL):c.4279+13G>A

gnomAD frequency: 0.00014  dbSNP: rs376435404
Minimum review status: Collection method:
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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 RCV001593342 SCV001816276 likely benign not provided 2020-09-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001593342 SCV002381128 benign not provided 2023-08-17 criteria provided, single submitter clinical testing

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