ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.-34T>C

dbSNP: rs2136102771
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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 RCV002153274 SCV002452106 likely benign Fanconi anemia 2023-10-04 criteria provided, single submitter clinical testing

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