ClinVar Miner

Submissions for variant NM_005609.4(PYGM):c.1358_1364del (p.Val453fs)

dbSNP: rs2135833005
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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 RCV002007330 SCV002230689 pathogenic Glycogen storage disease, type V 2021-05-16 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Val453Alafs*84) in the PYGM gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in PYGM are known to be pathogenic (PMID: 8316268, 16786513). This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with PYGM-related conditions. For these reasons, this variant has been classified as Pathogenic.

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