ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.457-12T>A

gnomAD frequency: 0.00003  dbSNP: rs188659251
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001720102 SCV000520576 likely benign not provided 2020-02-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002062418 SCV002328675 likely benign Fanconi anemia 2025-01-12 criteria provided, single submitter clinical testing

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