ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.904+34T>C

gnomAD frequency: 0.30375  dbSNP: rs28363318
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001713676 SCV001945709 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001796701 SCV002033419 benign Fanconi anemia complementation group O 2021-11-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001713676 SCV005252836 benign not provided criteria provided, single submitter not provided
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute RCV001682699 SCV001905782 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001682699 SCV001955278 benign not specified no assertion criteria provided clinical testing

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