ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.1299T>C (p.Pro433=)

dbSNP: rs761685061
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Total submissions: 2
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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 RCV001170175 SCV001332725 benign Cardiomyopathy 2019-04-23 criteria provided, single submitter clinical testing
Institute of Human Genetics, University of Wuerzburg RCV004596411 SCV005088681 not provided Hypertrophic cardiomyopathy 2 no assertion provided clinical testing

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