ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.274-6_274-4del

gnomAD frequency: 0.00004  dbSNP: rs762278011
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001428187 SCV001630880 likely benign Fanconi anemia 2023-09-21 criteria provided, single submitter clinical testing

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