{{Rsnum
|rsid=121918057
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=UROD
|position=45014803
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=UROD
}}{{omim
|id=613521
|rsnum=121918057
|variant=0002
}}{{ClinVar
|rsid=121918057
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=45014803
|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; 2
|CLNHGVS=NC_000001.11:g.45014803G>A; NC_000001.11:g.45014803G>T
|CLNORIGIN=1
|CLNSRCID=
NM_000374.4:c.842G>A; NR_036510.1:n.1025G>A; 613521.0002; NM_000374.4:c.842G>T; NR_036510.1:n.1025G>T; 613521.0001
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000000083.1; RCV000024023.1; RCV000000082.2
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDBN=Hepatoerythropoietic porphyria; Porphyria cutanea tarda; Familial porphyria cutanea tarda
|CLNDSDB=MedGen; MedGen:SNOMED_CT; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0162569; C0162566:61860000; C0268323:176100:ORPHA101330:59229005
|CLNSRC=ClinVar; OMIM Allelic Variant
|Disease=Hepatoerythropoietic porphyria; Porphyria cutanea tarda; Familial porphyria cutanea tarda
}}