{{Rsnum
|rsid=387906673
|Chromosome=6
|position=131874314
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ENPP1
|Gene_s=ENPP1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=6
|CLNACC=RCV000022721.18
|CLNALLE=1
|CLNDBN=Arterial calcification of infancy
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1859727:208000:51608
|CLNHGVS=NC_000006.11:g.132195454G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=173335.0017
|Disease=Arterial calcification of infancy
|FwdALT=C
|FwdREF=G
|REF=G
|RSPOS=132195454
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906673
|GENEINFO=ENPP1:5167
|GENE_ID=5167
|GENE_NAME=ENPP1
}}