{{Rsnum
|rsid=121918065
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=UROD
|position=45014976
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=UROD
}}{{omim
|id=613521
|rsnum=121918065
|variant=0011
}}{{ClinVar
|rsid=121918065
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=45014976
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=UROD:7389
|GENE_NAME=UROD
|GENE_ID=7389
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.45014976C>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000374.4:c.912C>A; NR_036510.1:n.1095C>A; 613521.0011
|CLNSIG=5
|CLNCUI=C0268323
|CLNDBN=Familial porphyria cutanea tarda
|Disease=Familial porphyria cutanea tarda
|CLNACC=RCV000000093.2
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268323:176100:ORPHA101330:59229005
}}