{{Rsnum
|rsid=121909579
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CP
|position=149179587
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CP
}}{{omim
|id=117700
|rsnum=121909579
|variant=0003
}}{{ClinVar
|rsid=121909579
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=148897374
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CP:1356
|GENE_NAME=CP
|GENE_ID=1356
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.148897374C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1493; 117700.0003
|CLNSIG=5
|CLNCUI=C0878682
|CLNDBN=Deficiency of ferroxidase; Hypoceruloplasminemia
|Disease=Deficiency of ferroxidase; Hypoceruloplasminemia
|CLNACC=RCV000019120.27; RCV000019121.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1493:C0878682:604290:48818:124224004; C1858582
}}