ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.1656T>C (p.Phe552=)

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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 RCV003636842 SCV004540225 likely benign Fanconi anemia 2023-08-07 criteria provided, single submitter clinical testing

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