List of variants reported as benign for disorder of glycogen metabolism by Phosphorus, Inc.

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000642.3(AGL):c.894C>T (p.Leu298=)	rs2230306	0.76251
NM_000152.5(GAA):c.324T>C (p.Cys108=)	rs1800300	0.71989
NM_000642.3(AGL):c.2812+11G>A	rs555929	0.65828
NM_000152.5(GAA):c.596A>G (p.His199Arg)	rs1042393	0.65667
NM_000152.5(GAA):c.1203G>A (p.Gln401=)	rs1800304	0.65453
NM_000642.3(AGL):c.-10A>G	rs2307130	0.41188
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.921A>T (p.Ala307=)	rs1800303	0.11304
NM_000152.5(GAA):c.1374C>T (p.Tyr458=)	rs1800305	0.10079
NM_000152.5(GAA):c.2446G>A (p.Val816Ile)	rs1800314	0.05752
NM_000152.5(GAA):c.*3G>A	rs1800317	0.05534
NM_000152.5(GAA):c.2780C>T (p.Thr927Ile)	rs1800315	0.04402
NM_000642.3(AGL):c.686A>G (p.Gln229Arg)	rs17121403	0.04398
NM_000152.3(GAA):c.2065G>A (p.Glu689Lys)	rs1800309	0.04051
NM_000152.5(GAA):c.858+7_858+8insAGCGGGC	rs3071247

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