ClinVar Miner

Submissions for variant NM_001018005.2(TPM1):c.563+10C>T

dbSNP: rs397516377
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Total submissions: 3
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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 RCV000036344 SCV000059996 likely benign not specified 2008-03-01 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003149626 SCV003837750 uncertain significance Cardiomyopathy 2021-10-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005089348 SCV005767601 likely benign Hypertrophic cardiomyopathy 2024-02-19 criteria provided, single submitter clinical testing

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