{{Rsnum
|rsid = 28934904
|Gene = MECP2
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=X
|position=154031431
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MECP2
}}{{omim
|desc=RETT SYNDROME
|id=300005
|rsnum=28934904
|variant=0001
}}
{{ neighbor
| rsid = 28934908
| distance = 22
}}

{{ neighbor
| rsid = 28934907
| distance = 837
}}

{{ClinVar
|rsid=28934904
|Reversed=1
|FwdREF=C
|FwdALT=G,T
|REF=G
|ALT=A,C
|RSPOS=153296882
|CHROM=X
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=MECP2:4204
|GENE_NAME=MECP2
|GENE_ID=4204
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153296882G>A
|CLNSRC=Emory University; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=9525; NBK1497; 300005.0001
|CLNSIG=5
|CLNCUI=C0035372; C0035372,.
|CLNDBN=Rett syndrome, zappella variant; Rett's disorder; not provided
|Disease=Rett syndrome; Rett's disorder; not provided
|CLNACC=RCV000012578.22; RCV000030666.20; RCV000081202.1
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=C2677682; NBK1497:C0035372:312750:3095:778:68618008
}}

{{PMID Auto
|PMID=17387578
|Title=Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms.
}}

{{PMID Auto
|PMID=10508514
|Title=Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
}}

{{PMID Auto
|PMID=12746406
|Title=Patients with the R133C mutation: is their phenotype different from patients with Rett syndrome with other mutations?
|OA=1
}}

{{PMID Auto
|PMID=18332345
|Title=Investigating genotype-phenotype relationships in Rett syndrome using an international data set.
}}

{{PMID Auto
|PMID=18562141
|Title=Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant).
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}