ClinVar Miner

Submissions for variant NM_002906.4(RDX):c.1091-10T>C

dbSNP: rs876657572
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000222992 SCV000270792 likely benign not specified 2015-09-14 criteria provided, single submitter clinical testing c.1091-10T>C in intron 10 of RDX: This variant is not expected to have clinical significance because a T>C change at this position does not diverge from the spl ice consensus sequence and is therefore unlikely to impact splicing.

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