ClinVar Miner

Submissions for variant NC_000009.12:g.(?_95149913)_(95172157_?)del

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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 RCV001031685 SCV001194991 pathogenic Fanconi anemia 2019-04-05 criteria provided, single submitter clinical testing This variant is an out-of-frame deletion of the genomic region encompassing exons 5-7 of the FANCC gene. This is expected to create a premature translational stop signal and result in an absent or disrupted protein product. This variant has not been reported in the literature in individuals with FANCC-related conditions. Loss-of-function variants in FANCC are known to be pathogenic (PMID: 17924555). For these reasons, this variant has been classified as Pathogenic.

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