{{Rsnum
|rsid=267606828
|Chromosome=14
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FOXG1
|position=28767922
|Gene_s=FOXG1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=14
|CLNACC=RCV000014884.24
|CLNALLE=1
|CLNDBN=Rett syndrome, congenital variant
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3150705:613454:3095
|CLNHGVS=NC_000014.8:g.29237128T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=164874.0004
|Disease=Rett syndrome
|FwdALT=C
|FwdREF=T
|GENEINFO=FOXG1:2290
|GENE_ID=2290
|GENE_NAME=FOXG1
|REF=T
|RSPOS=29237128
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606828
}}