ClinVar Miner

Submissions for variant NM_005676.5(RBM10):c.2379A>C (p.Arg793=)

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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 RCV002928268 SCV003267606 benign not provided 2022-12-29 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003906350 SCV004730361 likely benign RBM10-related disorder 2022-05-09 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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