List of variants in gene GAA reported as benign by Genetic Services Laboratory, University of Chicago

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000152.5(GAA):c.2338G>A (p.Val780Ile)	rs1126690	0.71839
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.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.921A>T (p.Ala307=)	rs1800303	0.11304
NM_000152.5(GAA):c.1374C>T (p.Tyr458=)	rs1800305	0.10079
NM_000152.5(GAA):c.447G>A (p.Thr149=)	rs2289536	0.00362
NM_000152.5(GAA):c.858+8G>A	rs5822325	0.00055
NM_000152.5(GAA):c.858+7_858+8insAGCGGGC	rs3071247

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