{{Rsnum
|rsid=398122908
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HCFC1
|position=153971810
|Gene_s=HCFC1,TMEM187
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=X
|CLNACC=RCV000032896.24
|CLNALLE=1
|CLNDBN=X-linked mental retardation 3
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0796208:309541:369962
|CLNHGVS=NC_000023.10:g.153237261A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300019.0001
|Disease=X-linked mental retardation 3
|FwdALT=G
|FwdREF=A
|GENEINFO=TMEM187:8269; HCFC1:3054
|GENE_ID=8269; 3054
|GENE_NAME=TMEM187; HCFC1
|REF=A
|RSPOS=153237261
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=398122908
}}