{{Rsnum
|rsid=61753971
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MECP2
|position=154030546
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MECP2
}}{{omim
|id=300005
|rsnum=61753971
|variant=0023
}}

{{ClinVar
|rsid=61753971
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=153295997
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=MECP2:4204
|GENE_NAME=MECP2
|GENE_ID=4204
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153295997C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000012604.13
|CLNDBN=Encephalopathy, neonatal severe, due to mecp2 mutation
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300005.0023
|Disease=Encephalopathy
}}

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