{{Rsnum
|rsid=104894092
|Chromosome=8
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TNFRSF11B
|position=118932982
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNFRSF11B
}}{{omim
|id=602643
|rsnum=104894092
|variant=0004
}}{{ClinVar
|rsid=104894092
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=119945221
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TNFRSF11B:4982
|GENE_NAME=TNFRSF11B
|GENE_ID=4982
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.119945221A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602643.0004
|CLNSIG=5
|CLNCUI=C0268414
|CLNDBN=Hyperphosphatasemia with bone disease
|Disease=Hyperphosphatasemia with bone disease
|CLNACC=RCV000007386.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268414:239000:2801:9723006
}}