ClinVar Miner

Submissions for variant NM_001018005.2(TPM1):c.563+249C>T

dbSNP: rs397516379
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Total submissions: 2
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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 RCV000036346 SCV000059998 uncertain significance not specified 2010-05-20 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002504886 SCV002797662 uncertain significance Hypertrophic cardiomyopathy 3; Dilated cardiomyopathy 1Y 2021-08-18 criteria provided, single submitter clinical testing

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