{{Rsnum
|rsid=61748392
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MECP2
|position=154031418
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MECP2
}}{{omim
|id=300005
|rsnum=61748392
|variant=0017
}}

{{ClinVar
|rsid=61748392
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=153296869
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=MECP2:4204
|GENE_NAME=MECP2
|GENE_ID=4204
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153296869T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300005.0017
|CLNSIG=5
|CLNCUI=C1968550
|CLNDBN=Mental retardation, X-linked, syndromic 13
|Disease=Mental retardation
|CLNACC=RCV000012598.16
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1968550:300055:3077
}}

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