ClinVar Miner

Submissions for variant NM_133510.4(RAD51B):c.316-10_316-3dup

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003411041 SCV004136224 benign not provided 2022-06-01 criteria provided, single submitter clinical testing RAD51B: BS1, BS2
PreventionGenetics, part of Exact Sciences RCV003919117 SCV004737157 likely benign RAD51B-related disorder 2020-05-22 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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