{{Rsnum
|rsid=121918524
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PHF8
|position=54011232
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PHF8
}}{{omim
|id=300560
|rsnum=121918524
|variant=0004
}}{{ClinVar
|rsid=121918524
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=54037665
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PHF8:23133
|GENE_NAME=PHF8
|GENE_ID=23133
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.54037665A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300560.0004
|CLNSIG=5
|CLNCUI=C1846055
|CLNDBN=Siderius X-linked mental retardation syndrome
|Disease=Siderius X-linked mental retardation syndrome
|CLNACC=RCV000011547.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1846055:300263:85287
}}