ClinVar Miner

Submissions for variant NM_001393586.1(MYO7B):c.2826G>A (p.Ser942=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV003967391 SCV004793286 benign MYO7B-related disorder 2023-11-21 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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