ClinVar Miner

Submissions for variant NM_002906.4(RDX):c.1588-7dup

dbSNP: rs1864658406
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005103105 SCV005823925 benign not provided 2024-03-02 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003977033 SCV004795749 likely benign RDX-related disorder 2019-03-18 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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