ClinVar Miner

Submissions for variant NM_001018113.3(FANCB):c.1521A>T (p.Ser507=)

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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 RCV003522231 SCV004272900 likely benign Fanconi anemia 2023-04-04 criteria provided, single submitter clinical testing

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