ClinVar Miner

Submissions for variant NM_030653.4(DDX11):c.2271+18G>A

gnomAD frequency: 0.53832  dbSNP: rs10771803
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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 RCV001661384 SCV001876618 benign Warsaw breakage syndrome 2021-07-30 criteria provided, single submitter clinical testing
GeneDx RCV001685559 SCV001896024 benign not provided 2020-07-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001685559 SCV005236914 benign not provided criteria provided, single submitter not provided

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