ClinVar Miner

Submissions for variant NM_002473.6(MYH9):c.2807C>T (p.Ala936Val)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002288147 SCV002578734 uncertain significance not provided 2022-04-05 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 RCV002288147 SCV004252729 benign not provided 2023-06-04 criteria provided, single submitter clinical testing

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