ClinVar Miner

Submissions for variant NM_030653.4(DDX11):c.1983C>T (p.Leu661=)

gnomAD frequency: 0.53295  dbSNP: rs1046456
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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 RCV001661382 SCV001876615 benign Warsaw breakage syndrome 2021-07-30 criteria provided, single submitter clinical testing
GeneDx RCV001685558 SCV001905170 benign not provided 2019-08-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001685558 SCV005236910 benign not provided criteria provided, single submitter not provided

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