ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.3408+16A>G

gnomAD frequency: 0.00006  dbSNP: rs373636902
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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 RCV002078503 SCV002378451 likely benign Fanconi anemia 2025-02-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494152 SCV002802616 likely benign Fanconi anemia complementation group A 2022-05-07 criteria provided, single submitter clinical testing

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