{{Rsnum
|rsid=61751362
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MECP2
|position=154030948
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MECP2
}}{{omim
|id=300005
|rsnum=61751362
|variant=0011
}}

{{ClinVar
|rsid=61751362
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=153296399
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=MECP2:4204
|GENE_NAME=MECP2
|GENE_ID=4204
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153296399G>A
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=1187; 300005.0011
|CLNSIG=255
|CLNCUI=C0035372; C1845336,.
|CLNDBN=Rett's disorder; Autism, susceptibility to, X-linked 3; not provided
|Disease=Rett's disorder; Autism; not provided
|CLNACC=RCV000012590.18; RCV000012591.1; RCV000081215.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; MedGen:OMIM
|CLNDSDBID=NBK1497:C0035372:312750:3095:778:68618008; C1845336:300496
}}

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