ClinVar Miner

Submissions for variant NM_001018113.3(FANCB):c.2373C>G (p.Ser791Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003147173 SCV003833906 uncertain significance Fanconi anemia complementation group B 2023-05-12 criteria provided, single submitter clinical testing

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