ClinVar Miner

Submissions for variant NM_002473.6(MYH9):c.2976+9C>T

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002283429 SCV002572047 likely benign not specified 2024-12-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003096364 SCV003493905 likely benign not provided 2024-11-05 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004545278 SCV004761997 likely benign MYH9-related disorder 2021-06-15 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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