ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.3720+14A>G

dbSNP: rs200012909
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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 RCV001510130 SCV001717079 benign Fanconi anemia 2024-12-17 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495783 SCV002799083 likely benign Fanconi anemia complementation group I 2021-07-23 criteria provided, single submitter clinical testing

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