ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.-52C>T

gnomAD frequency: 0.00001  dbSNP: rs2136102913
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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 RCV001428686 SCV001631392 likely benign Fanconi anemia 2021-12-23 criteria provided, single submitter clinical testing

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