{{Rsnum
|rsid=121908020
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=UROS
|position=125788993
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=UROS
}}{{omim
|id=606938
|rsnum=121908020
|variant=0017
}}{{ClinVar
|rsid=121908020
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=127477562
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=UROS:7390
|GENE_NAME=UROS
|GENE_ID=7390
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.127477562C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK154652; 606938.0017
|CLNSIG=5
|CLNCUI=C0162530
|CLNDBN=Congenital erythropoietic porphyria
|Disease=Congenital erythropoietic porphyria
|CLNACC=RCV000003964.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK154652:C0162530:263700:79277
}}