Variants in gene FOXG1 with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005249.5(FOXG1):c.565C>G (p.Leu189Val)	rs1555321308
NM_005249.5(FOXG1):c.620T>C (p.Ile207Thr)	rs1881803464
NM_005249.5(FOXG1):c.681C>G (p.Asn227Lys)	rs786205012
NM_005249.5(FOXG1):c.701C>T (p.Ser234Phe)	rs1555321334
NM_005249.5(FOXG1):c.824G>C (p.Arg275Pro)	rs1555321361

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