ClinVar Miner

Submissions for variant NM_018062.4(FANCL):c.471+12G>A

gnomAD frequency: 0.00003  dbSNP: rs369756342
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002090390 SCV002325828 likely benign Fanconi anemia 2023-12-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002486805 SCV002801275 likely benign Fanconi anemia complementation group L 2021-10-01 criteria provided, single submitter clinical testing

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