Variants in gene FOXG1 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_005249.5(FOXG1):c.221C>A (p.Pro74Gln)	rs796052452	0.01958
NM_005249.5(FOXG1):c.209A>C (p.Gln70Pro)	rs587783633	0.00026
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.218A>C (p.Gln73Pro)	rs760663911	0.00015
NM_005249.5(FOXG1):c.594C>G (p.Pro198=)	rs141088742	0.00010
NM_005249.5(FOXG1):c.326C>T (p.Pro109Leu)	rs398124203	0.00002
NM_005249.5(FOXG1):c.1058A>G (p.Asn353Ser)	rs749879411	0.00001
NM_005249.5(FOXG1):c.1086G>A (p.Leu362=)	rs570981209
NM_005249.5(FOXG1):c.194CGC[6] (p.Pro69dup)	rs761703699
NM_005249.5(FOXG1):c.209AGC[5] (p.Gln73dup)	rs398124201
NM_005249.5(FOXG1):c.209_235del (p.Gln70_Pro78del)	rs587783634
NM_005249.5(FOXG1):c.219GCC[7] (p.Pro80dup)	rs786200975
NM_005249.5(FOXG1):c.237_239del (p.Pro80del)
NM_005249.5(FOXG1):c.344C>T (p.Ala115Val)	rs796052454
NM_005249.5(FOXG1):c.672C>G (p.Gly224=)	rs587783639

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