ClinVar Miner

Submissions for variant NM_020884.7(MYH7B):c.2355C>T (p.Asp785=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003541845 SCV004245442 likely benign not provided 2024-09-05 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003929204 SCV004737564 likely benign MYH7B-related disorder 2019-09-17 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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