ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.1414-4A>G

gnomAD frequency: 0.00001  dbSNP: rs781613701
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001407696 SCV001609675 likely benign Fanconi anemia 2022-08-16 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002488224 SCV002800012 likely benign Fanconi anemia complementation group D2 2021-09-23 criteria provided, single submitter clinical testing

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