{{Rsnum
|rsid = 28935468
|Gene = MECP2
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=X
|position=154030912
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MECP2
}}{{omim
|desc=RETT SYNDROME
|id=300005
|rsnum=28935468
|variant=0016
}}
{{ neighbor
| rsid = 28935200
| distance = 4391
}}

{{ neighbor
| rsid = 28934906
| distance = 443
}}

{{ClinVar
|rsid=28935468
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=153296363
|CHROM=X
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050168000000000502110100
|GENEINFO=MECP2:4204
|GENE_NAME=MECP2
|GENE_ID=4204
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153296363G>A
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=1203; 300005.0016
|CLNSIG=5
|CLNCUI=C0035372
|CLNDBN=Rett's disorder; not provided
|Disease=Rett's disorder; not provided
|CLNACC=RCV000012597.20; RCV000081218.1
|Tags=RV;PM;PMC;SLO;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=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.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}