List of variants in gene FOXG1 reported as pathogenic 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_005249.5(FOXG1):c.135_136dup (p.Gln46fs)	rs587783629
NM_005249.5(FOXG1):c.170_179del (p.His57fs)	rs587783631
NM_005249.5(FOXG1):c.256C>T (p.Gln86Ter)	rs398124202
NM_005249.5(FOXG1):c.256del (p.Gln86fs)	rs786205001
NM_005249.5(FOXG1):c.263_278del (p.Arg88fs)	rs587783635
NM_005249.5(FOXG1):c.298del (p.Gln100fs)	rs587783636
NM_005249.5(FOXG1):c.460dup (p.Glu154fs)	rs398124204
NM_005249.5(FOXG1):c.505_506delinsC (p.Gly169fs)	rs786205003
NM_005249.5(FOXG1):c.505_506delinsT (p.Gly169fs)	rs786205003
NM_005249.5(FOXG1):c.590G>T (p.Ser197Ile)	rs1881802605
NM_005249.5(FOXG1):c.757A>G (p.Asn253Asp)	rs587783641
NM_005249.5(FOXG1):c.762C>G (p.Tyr254Ter)	rs587783642
NM_005249.5(FOXG1):c.765G>T (p.Trp255Cys)	rs121913678

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