ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.1581+15A>G

dbSNP: rs1199408690
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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 RCV002085987 SCV002388497 likely benign Fanconi anemia 2021-07-02 criteria provided, single submitter clinical testing

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