List of variants in gene GAA reported as not provided for Glycogen storage disease, type II

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000152.5(GAA):c.271G>A (p.Asp91Asn)	rs1800299	0.02215
NM_000152.5(GAA):c.1726G>A (p.Gly576Ser)	rs1800307	0.00653
NM_000152.5(GAA):c.-32-13T>G	rs386834236	0.00384
NM_000152.5(GAA):c.2560C>T (p.Arg854Ter)	rs121907943	0.00063
NM_000152.5(GAA):c.525del (p.Glu176fs)	rs386834235	0.00019
NM_000152.5(GAA):c.1935C>A (p.Asp645Glu)	rs28940868	0.00004
NM_000152.5(GAA):c.670C>T (p.Arg224Trp)	rs757700700	0.00001
NM_000152.5(GAA):c.1192C>A (p.Leu398Met)	rs369707231
NM_000152.5(GAA):c.2483_2646+1del	rs1555603048

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