{{Rsnum
|rsid=137852216
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FAM123B
|position=64192230
|Gene_s=FAM123B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300647
|variant=0004
|rsnum=137852216
}}{{ClinVar
|rsid=137852216
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=63412110
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=AMER1:139285
|GENE_NAME=AMER1
|GENE_ID=139285
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.63412110G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300647.0004
|CLNSIG=5
|CLNCUI=C0432268
|CLNDBN=Osteopathia striata with cranial sclerosis
|Disease=Osteopathia striata with cranial sclerosis
|CLNACC=RCV000011453.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0432268:300373:2780:254129003
}}