ClinVar Miner

Submissions for variant NM_000289.6(PFKM):c.937-8T>C

dbSNP: rs2135956395
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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 RCV001432605 SCV001635377 likely benign Glycogen storage disease, type VII 2020-02-18 criteria provided, single submitter clinical testing

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