ClinVar Miner

Submissions for variant NM_021922.3(FANCE):c.1378C>G (p.Arg460Gly)

dbSNP: rs200535245
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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 RCV002132277 SCV002401734 benign Fanconi anemia complementation group E 2024-02-14 criteria provided, single submitter clinical testing

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