Variants in gene FOXG1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 14

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HGVS	dbSNP	gnomAD frequency
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.503G>C (p.Gly168Ala)	rs148157138	0.00048
NM_005249.5(FOXG1):c.201G>T (p.Pro67=)	rs587780944	0.00029
NM_005249.5(FOXG1):c.1323C>T (p.Ser441=)	rs144434028	0.00023
NM_005249.5(FOXG1):c.456G>T (p.Gly152=)	rs587783637	0.00020
NM_005249.5(FOXG1):c.*4C>T	rs774917687	0.00012
NM_005249.5(FOXG1):c.1161G>A (p.Ser387=)	rs147154860	0.00012
NM_005249.5(FOXG1):c.165C>T (p.His55=)	rs796052449	0.00004
NM_005249.5(FOXG1):c.326C>T (p.Pro109Leu)	rs398124203	0.00002
NM_005249.5(FOXG1):c.141CCA[8] (p.His57dup)	rs587783630
NM_005249.5(FOXG1):c.209AGC[5] (p.Gln73dup)	rs398124201
NM_005249.5(FOXG1):c.209_232del (p.Gln70_Pro77del)	rs794726920
NM_005249.5(FOXG1):c.219GCC[7] (p.Pro80dup)	rs786200975

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