ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.1464T>G (p.Pro488=)

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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 RCV002721377 SCV003000377 likely benign Fanconi anemia 2021-12-19 criteria provided, single submitter clinical testing

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