ClinVar Miner

Submissions for variant NM_015164.4(PLEKHM2):c.652+11C>G

dbSNP: rs2148361251
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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 RCV002078209 SCV002377841 likely benign Dilated Cardiomyopathy, Recessive 2021-08-23 criteria provided, single submitter clinical testing

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