ClinVar Miner

Submissions for variant NM_005159.5(ACTC1):c.570C>T (p.Tyr190=)

dbSNP: rs1595760934
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001176028 SCV001339841 likely benign Cardiomyopathy 2020-02-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001405108 SCV001607025 likely benign Hypertrophic cardiomyopathy 11; Dilated cardiomyopathy 1R; Atrial septal defect 5 2018-05-09 criteria provided, single submitter clinical testing

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