ClinVar Miner

Submissions for variant NM_015164.4(PLEKHM2):c.466-10C>G

gnomAD frequency: 0.00001  dbSNP: rs961545436
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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 RCV002188268 SCV002483559 likely benign Dilated Cardiomyopathy, Recessive 2023-01-11 criteria provided, single submitter clinical testing

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