ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.1382-5T>C

dbSNP: rs2151549574
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001829266 SCV002096971 uncertain significance Fanconi anemia complementation group I 2022-01-07 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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