ClinVar Miner

Submissions for variant NM_000294.3(PHKG2):c.327-7C>T

dbSNP: rs2053374794
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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 RCV003867090 SCV004670993 likely benign Glycogen storage disease IXc 2023-04-28 criteria provided, single submitter clinical testing

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