ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.784-9A>G

gnomAD frequency: 0.00001  dbSNP: rs1388537203
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001414787 SCV001616930 likely benign Fanconi anemia 2023-03-08 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002488230 SCV002796585 likely benign Fanconi anemia complementation group D2 2022-04-25 criteria provided, single submitter clinical testing

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