List of variants in gene GAA reported as benign by PreventionGenetics, part of Exact Sciences

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: 35

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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.2338G>A (p.Val780Ile)	rs1126690	0.71839
NM_000152.5(GAA):c.1327-18A>G	rs2278619	0.71811
NM_000152.5(GAA):c.1551+49C>A	rs2304843	0.66585
NM_000152.5(GAA):c.547-39T>G	rs12452721	0.65696
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.858+30T>C	rs2304845	0.65092
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.693-49C>T	rs78855075	0.09045
NM_000152.5(GAA):c.1754+12G>A	rs2304840	0.06396
NM_000152.5(GAA):c.2446G>A (p.Val816Ile)	rs1800314	0.05752
NM_000152.5(GAA):c.1636+43G>T	rs2304842	0.05728
NM_000152.5(GAA):c.*3G>A	rs1800317	0.05534
NM_000152.5(GAA):c.1888+21G>A	rs2304837	0.05276
NM_000152.5(GAA):c.2780C>T (p.Thr927Ile)	rs1800315	0.04402
NM_000152.3(GAA):c.2065G>A (p.Glu689Lys)	rs1800309	0.04051
NM_000152.5(GAA):c.271G>A (p.Asp91Asn)	rs1800299	0.02215
NM_000152.5(GAA):c.1075+13C>T	rs41292402	0.01065
NM_000152.5(GAA):c.1726G>A (p.Gly576Ser)	rs1800307	0.00653
NM_000152.5(GAA):c.852G>A (p.Ala284=)	rs142626724	0.00638
NM_000152.5(GAA):c.447G>A (p.Thr149=)	rs2289536	0.00362
NM_000152.5(GAA):c.257C>G (p.Pro86Arg)	rs2229222	0.00038
NM_000152.5(GAA):c.2668G>C (p.Val890Leu)	rs377286472	0.00002
NM_000152.5(GAA):c.858+7_858+8insAGCGGGC	rs3071247

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