ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.1554T>C (p.Ile518=)

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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 RCV005143862 SCV005765058 likely benign Fanconi anemia 2024-08-27 criteria provided, single submitter clinical testing

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