ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.165+17A>G

gnomAD frequency: 0.00002  dbSNP: rs1046183823
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002200884 SCV002488831 likely benign Fanconi anemia 2025-02-04 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500403 SCV002804748 likely benign Fanconi anemia complementation group C 2021-11-27 criteria provided, single submitter clinical testing

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