ClinVar Miner

Submissions for variant NM_001018005.2(TPM1):c.150C>A (p.Leu50=)

dbSNP: rs2140627934
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001805395 SCV002052610 likely benign Cardiomyopathy 2021-05-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002074196 SCV002490689 likely benign Hypertrophic cardiomyopathy 2021-10-27 criteria provided, single submitter clinical testing

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