ClinVar Miner

Submissions for variant NM_030653.4(DDX11):c.639-10A>T

gnomAD frequency: 0.53173  dbSNP: rs7308754
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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 RCV000947443 SCV001093621 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001664563 SCV001876610 benign Warsaw breakage syndrome 2021-07-30 criteria provided, single submitter clinical testing
GeneDx RCV000947443 SCV001905312 benign not provided 2021-04-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000947443 SCV005236898 benign not provided criteria provided, single submitter not provided

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