ClinVar Miner

Submissions for variant NM_021922.3(FANCE):c.1182T>C (p.Tyr394=)

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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 RCV003510574 SCV004363931 likely benign Fanconi anemia complementation group E 2024-12-19 criteria provided, single submitter clinical testing

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