{{Rsnum
|rsid=397515351
|Chromosome=10
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=UROS
|position=125816722
|Gene_s=UROS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=10
|CLNACC=RCV000003963.2
|CLNALLE=1
|CLNDBN=Congenital erythropoietic porphyria
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK154652:C0162530:263700:79277
|CLNHGVS=NC_000010.10:g.127505291G>T
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK154652; 606938.0016
|Disease=Congenital erythropoietic porphyria
|FwdALT=A
|FwdREF=C
|GENEINFO=UROS:7390
|GENE_ID=7390
|GENE_NAME=UROS
|REF=G
|RSPOS=127505291
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397515351
}}