{{Rsnum
|rsid=104894343
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGF23
|position=4372622
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGF23
}}{{omim
|id=605380
|rsnum=104894343
|variant=0004
}}{{ClinVar
|rsid=104894343
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=4481788
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FGF23:8074
|GENE_NAME=FGF23
|GENE_ID=8074
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.4481788A>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000005331.1
|CLNDBN=Tumoral calcinosis, familial, hyperphosphatemic
|CLNDSDB=MedGen:OMIM:OMIM:Orphanet
|CLNDSDBID=C1876187:211900:610233:53715
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605380.0004
|Disease=Tumoral calcinosis
}}