ClinVar Miner

Submissions for variant NM_001356.5(DDX3X):c.104-10A>T

gnomAD frequency: 0.00708  dbSNP: rs112766093
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000882844 SCV001026106 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000882844 SCV001745626 likely benign not provided 2018-07-26 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495353 SCV002797831 likely benign Intellectual disability, X-linked 102 2021-08-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000882844 SCV005209266 likely benign not provided criteria provided, single submitter not provided

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