ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.3822T>C (p.Tyr1274=)

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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 RCV003067962 SCV003451072 likely benign Fanconi anemia 2021-12-17 criteria provided, single submitter clinical testing

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