{{Rsnum
|rsid=61751439
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MECP2
|position=154030919
|Gene_s=MECP2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=61751439
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=153296370
|CHROM=X
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050168000000000002100100
|GENEINFO=MECP2:4204
|GENE_NAME=MECP2
|GENE_ID=4204
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153296370G>C
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Rett's disorder
|Disease=Rett's disorder
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD
|CLNACC=RCV000030167.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1497:C0035372:312750:3095:778:68618008
}}

{{PMID Auto
|PMID=15173251
|Title=Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome: a cohort of 171 cases.
|OA=1
}}

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