ClinVar Miner

Submissions for variant NM_006790.3(MYOT):c.162CTC[1] (p.Ser56del)

dbSNP: rs777691147
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002300970 SCV002588262 uncertain significance not provided 2022-04-28 criteria provided, single submitter clinical testing In silico analysis supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge; This variant is associated with the following publications: (PMID: 22349301)

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