ClinVar Miner

Submissions for variant NM_000294.3(PHKG2):c.802-17C>T

gnomAD frequency: 0.00003  dbSNP: rs772388120
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000434901 SCV000532446 likely benign not specified 2016-10-14 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV002522534 SCV003250995 benign Glycogen storage disease IXc 2024-02-27 criteria provided, single submitter clinical testing

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