ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.228C>T (p.Cys76=)

dbSNP: rs2139101515
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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 RCV003636391 SCV004514280 likely benign Fanconi anemia 2023-01-18 criteria provided, single submitter clinical testing

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