ClinVar Miner

Submissions for variant NM_144573.4(NEXN):c.817del (p.Arg273fs)

dbSNP: rs2102125160
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001799384 SCV002043718 uncertain significance Cardiomyopathy 2020-10-28 criteria provided, single submitter clinical testing

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