ClinVar Miner

Submissions for variant NM_022725.4(FANCF):c.692G>A (p.Gly231Glu)

dbSNP: rs1858622610
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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 RCV001929107 SCV002204465 uncertain significance Fanconi anemia 2021-08-28 criteria provided, single submitter clinical testing

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