ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.3925-17A>G

dbSNP: rs1164805902
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002120246 SCV002407064 likely benign Fanconi anemia 2021-07-17 criteria provided, single submitter clinical testing

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