{{Rsnum
|rsid=387907269
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FAM123B
|position=64192476
|Gene_s=FAM123B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000030706.3
|CLNALLE=1
|CLNDBN=Osteopathia striata with cranial sclerosis
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0432268:300373:2780:254129003
|CLNHGVS=NC_000023.10:g.63412356G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300647.0008
|Disease=Osteopathia striata with cranial sclerosis
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=63412356
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907269
|GENEINFO=AMER1:139285
|GENE_ID=139285
|GENE_NAME=AMER1
}}