ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.1932T>C (p.His644=)

gnomAD frequency: 0.00001  dbSNP: rs1443665941
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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 RCV003524477 SCV004319342 likely benign Fanconi anemia 2023-05-11 criteria provided, single submitter clinical testing

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