ClinVar Miner

Submissions for variant NM_001018005.2(TPM1):c.294G>A (p.Glu98=)

dbSNP: rs747206706
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001177395 SCV001341593 likely benign Cardiomyopathy 2019-10-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068187 SCV002383567 likely benign Hypertrophic cardiomyopathy 2023-12-08 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003117806 SCV003800739 likely benign not specified 2023-01-09 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV002068187 SCV005426866 likely benign Hypertrophic cardiomyopathy 2024-05-24 criteria provided, single submitter clinical testing

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