List of variants in gene FOXG1 reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005249.5(FOXG1):c.1170C>A (p.Cys390Ter)	rs1392520466
NM_005249.5(FOXG1):c.1366_1375del (p.Arg457fs)
NM_005249.5(FOXG1):c.214C>T (p.Gln72Ter)	rs1555321237
NM_005249.5(FOXG1):c.256dup (p.Gln86fs)	rs786205001
NM_005249.5(FOXG1):c.460dup (p.Glu154fs)	rs398124204
NM_005249.5(FOXG1):c.85C>T (p.Gln29Ter)

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