ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.-71G>A

gnomAD frequency: 0.00001  dbSNP: rs1296685064
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000608577 SCV000716230 likely benign not specified 2017-02-22 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV001455080 SCV001658829 likely benign Fanconi anemia 2023-07-29 criteria provided, single submitter clinical testing

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