ClinVar Miner

Submissions for variant NM_144573.4(NEXN):c.*4CT[1]

dbSNP: rs553696163
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000402554 SCV000358997 uncertain significance Dilated Cardiomyopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000298933 SCV000358998 uncertain significance Hypertrophic cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV000768812 SCV000900185 uncertain significance Cardiomyopathy 2017-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001618514 SCV001846350 likely benign not provided 2018-09-11 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004701400 SCV005204787 benign not specified 2024-06-17 criteria provided, single submitter clinical testing

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