ClinVar Miner

Submissions for variant NM_001172309.1(NEXN):c.*4_*5CT[1] (rs553696163)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000402554 SCV000358997 uncertain significance Dilated Cardiomyopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,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

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