{{Rsnum
|rsid=137852213
|Chromosome=X
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=AP1S2
|position=15845965
|Gene_s=AP1S2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300629
|variant=0005
|rsnum=137852213
}}{{ClinVar
|rsid=137852213
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=15864088
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=AP1S2:8905
|GENE_NAME=AP1S2
|GENE_ID=8905
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.15864088C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300629.0005
|CLNSIG=5
|CLNCUI=C1845078
|CLNDBN=Mental retardation, X-linked, syndromic, fried type
|Disease=Mental retardation
|CLNACC=RCV000011528.3
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1845078:300630:85335
}}