ClinVar Miner

Submissions for variant NM_022725.4(FANCF):c.699G>A (p.Gly233=)

gnomAD frequency: 0.00001  dbSNP: rs1565055031
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001421951 SCV001624485 likely benign Fanconi anemia 2019-04-19 criteria provided, single submitter clinical testing

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