{{Rsnum
|rsid=121908249
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=ENPP1
|position=131890435
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ENPP1
}}{{omim
|id=173335
|rsnum=121908249
|variant=0013
}}{{ClinVar
|rsid=121908249
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=132211575
|CHROM=6
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=ENPP1:5167
|GENE_NAME=ENPP1
|GENE_ID=5167
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.132211575A>C
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=173335.0013; VAR_063720
|CLNSIG=5
|CLNCUI=C2750078
|CLNDBN=Hypophosphatemic rickets, autosomal recessive, 2
|Disease=Hypophosphatemic rickets
|CLNACC=RCV000014566.25
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2750078:613312:289176
}}{{PMID Auto
|PMID=20137772
|Title=Autosomal-recessive hypophosphatemic rickets is associated with an inactivation mutation in the ENPP1 gene.
|OA=1
}}