ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.3816+17_3816+19del

dbSNP: rs374324314
Minimum review status: Collection method:
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000287731 SCV000394227 uncertain significance Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000287731 SCV002347772 benign Fanconi anemia 2024-02-01 criteria provided, single submitter clinical testing

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