{{Rsnum
|rsid=121918060
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=UROD
|position=45013187
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HECTD3,UROD
}}{{omim
|id=613521
|rsnum=121918060
|variant=0006
}}{{ClinVar
|rsid=121918060
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=45013187
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260420a05000002110100
|GENEINFO=HECTD3:79654; UROD:7389
|GENE_NAME=HECTD3; UROD
|GENE_ID=79654; 7389
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.45013187C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000374.4:c.185C>T; NM_024602.5:c.-1930G>A; NR_036510.1:n.368C>T; 613521.0006
|CLNSIG=5
|CLNCUI=C0162569
|CLNDBN=Hepatoerythropoietic porphyria
|Disease=Hepatoerythropoietic porphyria
|CLNACC=RCV000000088.2
|Tags=PM;S3D;NSM;REF;U5;R5;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C0162569
}}