ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.710-20_710-19del

dbSNP: rs2040524550
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002075411 SCV002378121 likely benign Fanconi anemia 2023-11-02 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002486849 SCV002794742 likely benign Fanconi anemia complementation group A 2022-01-10 criteria provided, single submitter clinical testing

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