ClinVar Miner

Submissions for variant NM_014476.6(PDLIM3):c.331-16C>T

gnomAD frequency: 0.00028  dbSNP: rs200663921
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001719098 SCV000729444 likely benign not provided 2018-05-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002066701 SCV002404443 benign Primary dilated cardiomyopathy; Hypertrophic cardiomyopathy 2023-12-28 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003230553 SCV003928400 benign not specified 2023-04-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001719098 SCV005256781 likely benign not provided criteria provided, single submitter not provided

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