{{Rsnum
|rsid=318240758
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HCFC1
|position=153963263
|Gene_s=HCFC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=X
|CLNACC=RCV000032897.22; RCV000059786.1
|CLNALLE=1
|CLNDBN=X-linked mental retardation 3; not provided
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0796208:309541:369962
|CLNHGVS=NC_000023.10:g.153228714C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=300019.0002; VAR_069098
|Disease=X-linked mental retardation 3; not provided
|FwdALT=A
|FwdREF=G
|GENEINFO=HCFC1:3054
|GENE_ID=3054
|GENE_NAME=HCFC1
|REF=C
|RSPOS=153228714
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050168000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=318240758
}}