ClinVar Miner

Submissions for variant NM_003611.3(OFD1):c.412+264C>A

dbSNP: rs868585834
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001586717 SCV001820554 likely benign not provided 2019-08-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001586717 SCV005207980 likely benign not provided criteria provided, single submitter not provided

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