ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2853-4C>A

dbSNP: rs1289126600
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001437569 SCV001640425 likely benign Fanconi anemia 2022-11-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002504722 SCV002807434 likely benign Fanconi anemia complementation group A 2022-03-25 criteria provided, single submitter clinical testing

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