ClinVar Miner

Submissions for variant NM_002294.3(LAMP2):c.865-1G>C

dbSNP: rs397516752
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000037433 SCV000061090 likely pathogenic Hypertrophic cardiomyopathy 2009-02-11 no assertion criteria provided clinical testing

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