List of variants in gene FOXG1 reported as benign for not specified

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_005249.5(FOXG1):c.*13C>A	rs151157846	0.01290
NM_005249.5(FOXG1):c.1233G>A (p.Ala411=)	rs34654108	0.00801
NM_005249.5(FOXG1):c.447C>T (p.Ala149=)	rs112803404	0.00126
NM_005249.5(FOXG1):c.489C>T (p.Gly163=)	rs375378714	0.00062
NM_005249.5(FOXG1):c.1323C>T (p.Ser441=)	rs144434028	0.00023
NM_005249.5(FOXG1):c.1161G>A (p.Ser387=)	rs147154860	0.00012
NM_005249.5(FOXG1):c.594C>G (p.Pro198=)	rs141088742	0.00010
NM_005249.5(FOXG1):c.1399C>T (p.Leu467=)	rs371279404	0.00006
NM_005249.5(FOXG1):c.162T>C (p.His54=)	rs796052448	0.00004
NM_005249.5(FOXG1):c.165C>T (p.His55=)	rs796052449	0.00004
NM_005249.5(FOXG1):c.1218C>G (p.Ser406=)	rs587783628	0.00003
NM_005249.5(FOXG1):c.189G>T (p.Pro63=)	rs796052451	0.00002
NM_005249.5(FOXG1):c.326C>T (p.Pro109Leu)	rs398124203	0.00002
NM_005249.5(FOXG1):c.1086G>A (p.Leu362=)	rs570981209
NM_005249.5(FOXG1):c.141CCA[8] (p.His57dup)	rs587783630

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