ClinVar Miner

Submissions for variant NM_000294.3(PHKG2):c.326+15G>C

dbSNP: rs776831194
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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 RCV003626463 SCV004480903 likely benign Glycogen storage disease IXc 2023-12-03 criteria provided, single submitter clinical testing

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