ClinVar Miner

Submissions for variant NM_030653.4(DDX11):c.880+16A>G

gnomAD frequency: 0.53242  dbSNP: rs2075318
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001661381 SCV001876613 benign Warsaw breakage syndrome 2021-07-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707668 SCV005236903 benign not provided criteria provided, single submitter not provided

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