ClinVar Miner

Submissions for variant NM_015164.4(PLEKHM2):c.1831-10C>T

gnomAD frequency: 0.00001  dbSNP: rs750051545
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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 RCV002211468 SCV002358028 likely benign Dilated Cardiomyopathy, Recessive 2023-11-10 criteria provided, single submitter clinical testing

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