List of variants in gene combination DBNL, LOC129998343, PGAM2 reported as likely pathogenic for disorder of glycogen metabolism

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000290.4(PGAM2):c.233G>A (p.Trp78Ter)	rs10250779	0.00166
NM_000290.4(PGAM2):c.266A>C (p.Glu89Ala)	rs104894030	0.00007

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