ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2504+12_2504+14del

dbSNP: rs1023581563
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002105543 SCV002393204 likely benign Fanconi anemia 2023-11-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002479907 SCV002795647 likely benign Fanconi anemia complementation group A 2021-12-31 criteria provided, single submitter clinical testing

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