ClinVar Miner

Submissions for variant NM_005159.5(ACTC1):c.42C>T (p.Asn14=)

dbSNP: rs1257278537
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000779684 SCV000916413 likely benign not specified 2019-08-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067366 SCV002439581 likely benign Hypertrophic cardiomyopathy 11; Dilated cardiomyopathy 1R; Atrial septal defect 5 2022-09-13 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705780 SCV005214413 likely benign not provided criteria provided, single submitter not provided

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