ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.251-12T>G

dbSNP: rs1397340091
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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 RCV002190334 SCV002351010 likely benign Fanconi anemia 2021-06-20 criteria provided, single submitter clinical testing

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