ClinVar Miner

Submissions for variant NM_001018005.2(TPM1):c.645G>T (p.Ser215=)

dbSNP: rs773403386
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002103949 SCV002394967 likely benign Hypertrophic cardiomyopathy 2025-01-12 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV002103949 SCV004824571 likely benign Hypertrophic cardiomyopathy 2023-06-26 criteria provided, single submitter clinical testing

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