ClinVar Miner

Submissions for variant NM_022725.4(FANCF):c.807G>A (p.Ala269=)

gnomAD frequency: 0.00001  dbSNP: rs754312601
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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 RCV001822221 SCV002071462 likely benign not specified 2021-09-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002542497 SCV003496669 likely benign Fanconi anemia 2024-05-31 criteria provided, single submitter clinical testing

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