ClinVar Miner

Submissions for variant NM_018062.4(FANCL):c.776-10del

dbSNP: rs374236117
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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 RCV001520266 SCV001729327 benign Fanconi anemia 2025-01-14 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV001520266 SCV002527300 likely benign Fanconi anemia 2021-04-02 criteria provided, single submitter curation

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