ClinVar Miner

Submissions for variant NM_002473.6(MYH9):c.2976+10G>T

dbSNP: rs371839289
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001551432 SCV001771941 likely benign not provided 2018-09-07 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004542001 SCV004766318 likely benign MYH9-related disorder 2021-12-09 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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