{{Rsnum
|rsid = 28934905
|Gene = MECP2
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=X
|position=154031364
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MECP2
}}{{omim
|desc=RETT SYNDROME
|id=300005
|rsnum=28934905
|variant=0002
}}
{{ neighbor
| rsid = 28934906
| distance = 9
}}

{{ neighbor
| rsid = 28934908
| distance = 45
}}

{{ClinVar
|rsid=28934905
|Reversed=1
|FwdREF=T
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=153296815
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=MECP2:4204
|GENE_NAME=MECP2
|GENE_ID=4204
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000023.10:g.153296815A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300005.0002
|CLNSIG=5
|CLNCUI=C0035372
|CLNDBN=Rett's disorder
|Disease=Rett's disorder
|CLNACC=RCV000012579.18
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1497:C0035372:312750:3095:778:68618008
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}