ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.5103G>A (p.Gln1701=)

gnomAD frequency: 0.00001  dbSNP: rs1160184503
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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 RCV002090462 SCV002371032 likely benign Fanconi anemia 2021-03-29 criteria provided, single submitter clinical testing

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