ClinVar Miner

Submissions for variant NM_015164.4(PLEKHM2):c.258G>A (p.Val86=)

dbSNP: rs2148357794
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001409624 SCV001611656 likely benign Dilated Cardiomyopathy, Recessive 2019-04-01 criteria provided, single submitter clinical testing

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