List of variants reported as benign for lysosomal glycogen storage disease by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000152.5(GAA):c.2331+20G>A	rs2304832	0.80041
NM_000152.5(GAA):c.2040+20A>G	rs2304836	0.72004
NM_000152.5(GAA):c.324T>C (p.Cys108=)	rs1800300	0.71989
NM_000152.5(GAA):c.2338G>A (p.Val780Ile)	rs1126690	0.71839
NM_000152.5(GAA):c.1327-18A>G	rs2278619	0.71811
NM_000152.5(GAA):c.596A>G (p.His199Arg)	rs1042393	0.65667
NM_000152.5(GAA):c.547-4C>G	rs3816256	0.65665
NM_000152.5(GAA):c.668G>A (p.Arg223His)	rs1042395	0.65662
NM_000152.5(GAA):c.1438-19G>C	rs2304844	0.65495
NM_000152.5(GAA):c.955+12G>A	rs2252455	0.65487
NM_000152.5(GAA):c.1203G>A (p.Gln401=)	rs1800304	0.65453
NM_000152.5(GAA):c.2553G>A (p.Gly851=)	rs1042397	0.57872
NM_000152.5(GAA):c.2133A>G (p.Thr711=)	rs1800310	0.23591
NM_000152.5(GAA):c.1581G>A (p.Arg527=)	rs1042396	0.20175
NM_000152.5(GAA):c.642C>T (p.Ser214=)	rs1800301	0.16610
NM_000152.5(GAA):c.858+7_858+8insAGCGGGC	rs3071247
NM_002294.3(LAMP2):c.-32GTCGCCGCC[1]	rs193922648

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