ClinVar Miner

Submissions for variant NM_030653.4(DDX11):c.2223C>G (p.Ser741Arg)

dbSNP: rs151210946
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000224368 SCV000281278 likely benign not provided 2016-02-11 criteria provided, single submitter clinical testing Converted during submission to Likely benign.
Invitae RCV000224368 SCV001103849 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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