ClinVar Miner

Submissions for variant NM_005476.7(GNE):c.1633+14G>A

dbSNP: rs748208582
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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 RCV002185478 SCV002359331 likely benign GNE myopathy; Sialuria 2022-07-26 criteria provided, single submitter clinical testing

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