ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.2890-19G>A

gnomAD frequency: 0.00006  dbSNP: rs758850736
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002082018 SCV002423591 likely benign Fanconi anemia 2022-06-20 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500125 SCV002805273 likely benign Fanconi anemia complementation group I 2022-04-07 criteria provided, single submitter clinical testing

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