ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.165+18A>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003853074 SCV004652491 likely benign Fanconi anemia 2023-06-27 criteria provided, single submitter clinical testing

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