ClinVar Miner

Submissions for variant NM_000290.4(PGAM2):c.201C>T (p.Leu67=)

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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 RCV003857253 SCV004662172 likely benign Glycogen storage disease type X 2023-10-22 criteria provided, single submitter clinical testing

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