ClinVar Miner

Submissions for variant NM_001018005.2(TPM1):c.115-277G>A

dbSNP: rs1312883932
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001176595 SCV001340618 likely benign Cardiomyopathy 2019-09-10 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001700714 SCV001926093 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001724262 SCV001955418 likely benign not provided no assertion criteria provided clinical testing

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