List of variants in gene AGL reported as uncertain significance for Glycogen storage disease IIIa

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000642.3(AGL):c.3677T>C (p.Ile1226Thr)	rs749118487	0.00003
NM_000642.3(AGL):c.2113A>G (p.Ile705Val)	rs1570445259
NM_000642.3(AGL):c.847-3C>A	rs1571243667

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