ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.503-8T>C

dbSNP: rs1566516373
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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 RCV000770457 SCV000901900 uncertain significance Cardiomyopathy 2016-01-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001490669 SCV001695240 likely benign Hypertrophic cardiomyopathy 14 2022-08-23 criteria provided, single submitter clinical testing

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