ClinVar Miner

Submissions for variant NM_144573.4(NEXN):c.1922T>C (p.Leu641Ser)

dbSNP: rs760119697
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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 RCV000768809 SCV000900182 uncertain significance Cardiomyopathy 2018-07-30 criteria provided, single submitter clinical testing

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