{{Rsnum
|rsid=193922678
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MECP2
|position=154030387
|Gene_s=MECP2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922678
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=153295838
|CHROM=X
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050168000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153295838C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Rett's disorder
|Disease=Rett's disorder
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD
|CLNACC=RCV000030164.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1497:C0035372:312750:3095:778:68618008
|GENEINFO=MECP2:4204
|GENE_ID=4204
|GENE_NAME=MECP2
}}{{PMID Auto
|PMID=19495527
|Title=MECP2 mutations in Malaysian Rett syndrome patients.
}}