ClinVar Miner

Submissions for variant NM_005159.5(ACTC1):c.1050T>A (p.Ser350=)

dbSNP: rs895745627
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001679337 SCV001902957 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003771839 SCV004607195 likely benign Hypertrophic cardiomyopathy 11; Dilated cardiomyopathy 1R; Atrial septal defect 5 2023-10-06 criteria provided, single submitter clinical testing

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