ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.3622C>T (p.Leu1208=)

dbSNP: rs1448880215
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001820356 SCV002071131 uncertain significance not specified 2019-08-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001869718 SCV002247373 likely benign Fanconi anemia 2023-07-14 criteria provided, single submitter clinical testing

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