ClinVar Miner

Submissions for variant NM_001018005.2(TPM1):c.21G>A (p.Lys7=)

dbSNP: rs2140594266
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002083071 SCV002380502 likely benign Hypertrophic cardiomyopathy 2021-07-09 criteria provided, single submitter clinical testing

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