{{Rsnum
|rsid=61749715
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MECP2
|position=154031154
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MECP2
}}{{omim
|id=300005
|rsnum=61749715
|variant=0033
}}

{{ClinVar
|rsid=61749715
|Reversed=1
|FwdREF=C
|FwdALT=G,T
|REF=G
|ALT=A,C
|RSPOS=153296605
|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.153296605G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300005.0033
|CLNSIG=5
|CLNCUI=C1968550
|CLNDBN=Mental retardation, X-linked, syndromic 13
|Disease=Mental retardation
|CLNACC=RCV000012615.22
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1968550:300055:3077
}}

{{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}}