ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.882+15G>T

gnomAD frequency: 0.00016  dbSNP: rs199522855
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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 RCV002220918 SCV002361561 likely benign Fanconi anemia 2025-01-28 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005008454 SCV005631321 uncertain significance Fanconi anemia complementation group I 2024-04-23 criteria provided, single submitter clinical testing

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