{{Rsnum
|rsid=61748396
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MECP2
|position=154031405
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MECP2
}}{{omim
|id=300005
|rsnum=61748396
|variant=0025
}}

{{ClinVar
|rsid=61748396
|Reversed=1
|FwdREF=C
|FwdALT=A,G
|REF=G
|ALT=C,T
|RSPOS=153296856
|CHROM=X
|dbSNPBuildID=133
|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.153296856G>C
|CLNORIGIN=0
|CLNSRCID=
300005.0025
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000012606.21
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=Atypical Rett syndrome
|CLNDSDB=MedGen
|CLNDSDBID=C2748910
|CLNSRC=OMIM Allelic Variant
|Disease=Atypical Rett syndrome
}}

{{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}}