ClinVar Miner

Submissions for variant NM_000289.6(PFKM):c.543C>T (p.Ala181=)

dbSNP: rs1370905542
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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 RCV001425807 SCV001628445 likely benign Glycogen storage disease, type VII 2020-08-07 criteria provided, single submitter clinical testing

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