{{Rsnum
|rsid=121913678
|Chromosome=14
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FOXG1
|position=28768044
|Gene_s=FOXG1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=164874
|rsnum=121913678
|variant=0001
}}{{ClinVar
|rsid=121913678
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=29237250
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FOXG1:2290
|GENE_NAME=FOXG1
|GENE_ID=2290
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.29237250G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=164874.0001
|CLNSIG=5
|CLNCUI=C3150705
|CLNDBN=Rett syndrome, congenital variant
|Disease=Rett syndrome
|CLNACC=RCV000014881.24
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3150705:613454:3095
}}