ClinVar Miner

Submissions for variant NM_030653.4(DDX11):c.2053-15C>T

gnomAD frequency: 0.53829  dbSNP: rs7966272
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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 RCV001661383 SCV001876616 benign Warsaw breakage syndrome 2021-07-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707669 SCV005236911 benign not provided criteria provided, single submitter not provided

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