ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.405-8G>A

dbSNP: rs1431351072
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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 RCV000648276 SCV000770090 likely benign Fanconi anemia complementation group O 2017-11-02 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV004596314 SCV005090386 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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