ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.3765+16C>A

gnomAD frequency: 0.00001  dbSNP: rs745639466
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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 RCV002210296 SCV002367524 likely benign Fanconi anemia 2024-01-04 criteria provided, single submitter clinical testing

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