ClinVar Miner

Submissions for variant NM_001018005.1(TPM1):c.640_645del

dbSNP: rs1555409659
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Human Genetics, University of Leuven RCV000498322 SCV000579528 likely pathogenic Hypertrophic cardiomyopathy 2017-02-09 criteria provided, single submitter clinical testing ACMG score likely pathogenic

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