ClinVar Miner

Submissions for variant NM_005609.4(PYGM):c.627C>T (p.His209=)

dbSNP: rs2135839184
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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 RCV001436779 SCV001639623 likely benign Glycogen storage disease, type V 2019-09-22 criteria provided, single submitter clinical testing

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