{{Rsnum
|rsid=137852214
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ZDHHC9
|position=129823724
|Gene_s=ZDHHC9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300646
|variant=0003
|rsnum=137852214
}}{{ClinVar
|rsid=137852214
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=128957700
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ZDHHC9:51114
|GENE_NAME=ZDHHC9
|GENE_ID=51114
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.128957700G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300646.0003
|CLNSIG=5
|CLNCUI=C2749033; C0268151
|CLNDBN=Mental retardation, X-linked, syndromic, raymond type
|Disease=Mental retardation
|CLNACC=RCV000011457.4
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2749033:300799:163953
}}