ClinVar Miner

Submissions for variant NM_002294.3(LAMP2):c.107C>G (p.Ser36Ter)

dbSNP: rs2147287657
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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 RCV001799285 SCV002043164 pathogenic Cardiomyopathy 2020-03-02 criteria provided, single submitter clinical testing

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