ClinVar Miner

Submissions for variant NM_022725.4(FANCF):c.618G>C (p.Ala206=)

dbSNP: rs1056134185
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001500147 SCV001704929 likely benign Fanconi anemia 2022-03-05 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001818909 SCV002068641 uncertain significance not specified 2019-03-19 criteria provided, single submitter clinical testing

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