ClinVar Miner

Submissions for variant NM_014000.2(VCL):c.2427C>T (p.Ser809=) (rs183739128)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000621865 SCV000736865 likely benign Cardiovascular phenotype 2017-03-13 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Illumina Clinical Services Laboratory,Illumina RCV000275440 SCV000364937 uncertain significance Dilated Cardiomyopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000466939 SCV000559715 likely benign Dilated cardiomyopathy 1W 2017-10-30 criteria provided, single submitter clinical testing

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