{{Rsnum
|rsid=179363900
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MECP2
|position=154031374
|Gene_s=MECP2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=179363900
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=153296825
|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.153296825G>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000012618.22
|CLNDBN=Rett syndrome, zappella variant
|CLNDSDB=MedGen
|CLNDSDBID=C2677682
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300005.0036
|Disease=Rett syndrome
}}