ClinVar Miner

Submissions for variant NM_001018005.2(TPM1):c.773-5C>T

gnomAD frequency: 0.00002  dbSNP: rs754213660
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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 RCV002219949 SCV002378779 likely benign Hypertrophic cardiomyopathy 2024-06-17 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV005403180 SCV006064255 likely benign Cardiomyopathy 2024-09-16 criteria provided, single submitter clinical testing

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