ClinVar Miner

Submissions for variant NM_022725.4(FANCF):c.471C>A (p.Leu157=)

dbSNP: rs201136733
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002102732 SCV002389856 likely benign Fanconi anemia 2025-01-13 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002102732 SCV002530494 likely benign Fanconi anemia 2020-12-08 criteria provided, single submitter curation

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