ClinVar Miner

Submissions for variant NM_030653.4(DDX11):c.638+15G>A

gnomAD frequency: 0.47740  dbSNP: rs4931428
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001661378 SCV001876609 benign Warsaw breakage syndrome 2021-07-30 criteria provided, single submitter clinical testing
GeneDx RCV001762733 SCV001988800 benign not provided 2021-10-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001762733 SCV005236897 benign not provided criteria provided, single submitter not provided

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