{{Rsnum
|rsid=61749743
|Chromosome=X
|position=154031118
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=MECP2
|Gene_s=MECP2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000012620.22
|CLNALLE=1
|CLNDBN=Rett's disorder
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1497:C0035372:312750:3095:778:68618008
|CLNHGVS=NC_000023.10:g.153296569delC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300005.0038
|Disease=Rett's disorder
|FwdREF=G
|GENEINFO=MECP2:4204
|GENE_ID=4204
|GENE_NAME=MECP2
|REF=AC
|RSPOS=153296568
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;SLO;OTHERKG;LSD
|VC=DIV
|VP=0x050160000000000002100200
|WGT=0
|dbSNPBuildID=137
|rsid=61749743
}}