{{Rsnum
|rsid=121918058
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=UROD
|position=45013933
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=UROD
}}{{omim
|id=613521
|rsnum=121918058
|variant=0004
}}{{ClinVar
|rsid=121918058
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=45013933
|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.45013933G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000374.4:c.499G>A; NR_036510.1:n.682G>A; 613521.0004
|CLNSIG=5
|CLNCUI=C0162569
|CLNDBN=Hepatoerythropoietic porphyria
|Disease=Hepatoerythropoietic porphyria
|CLNACC=RCV000000086.2
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C0162569
}}