{{Rsnum
|rsid = 28934908
|Gene = MECP2
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=X
|position=154031409
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MECP2
}}{{omim
|desc=MENTAL RETARDATION, X-LINKED 16
|id=300005
|rsnum=28934908
|variant=0015
}}
{{ neighbor
| rsid = 28934905
| distance = 45
}}

{{ neighbor
| rsid = 28934904
| distance = 22
}}

{{ClinVar
|rsid=28934908
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=153296860
|CHROM=X
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=MECP2:4204
|GENE_NAME=MECP2
|GENE_ID=4204
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153296860G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1497; 300005.0015
|CLNSIG=5
|CLNCUI=C1968550; C0035372
|CLNDBN=Mental retardation, X-linked, syndromic 13; Rett's disorder
|Disease=Mental retardation; Rett's disorder
|CLNACC=RCV000012596.22; RCV000020628.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=C1968550:300055:3077; NBK1497:C0035372:312750:3095:778:68618008
}}

{{PMID Auto
|PMID=12325
|Title=Design of a standard protocol for the challenge testing of antimicrobial preservative solutions [proceedings].
}}

{{PMID Auto
|PMID=11007980
|Title=MECP2 mutation in male patients with non-specific X-linked mental retardation.
}}

{{PMID Auto
|PMID=11309367
|Title=MECP2 is highly mutated in X-linked mental retardation.
}}

{{PMID Auto
|PMID=11772708
|Title=MECP2 mutation in a boy with language disorder and schizophrenia.
}}

{{PMID Auto
|PMID=11805248
|Title=A Rett syndrome MECP2 mutation that causes mental retardation in men.
}}

{{PMID Auto
|PMID=11885030
|Title=A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome.
|OA=1
}}

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