ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.948C>A (p.Ser316=)

dbSNP: rs2131055519
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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 RCV001822537 SCV002065295 likely benign not specified 2021-06-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003523111 SCV004369538 likely benign Fanconi anemia 2023-09-29 criteria provided, single submitter clinical testing

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