{{Rsnum
|rsid=121908017
|Chromosome=10
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=UROS
|position=125794978
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=UROS
}}{{omim
|id=606938
|rsnum=121908017
|variant=0010
}}
{{omim
|id=606938
|rsnum=121908017
|variant=0012
}}{{ClinVar
|rsid=121908017
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=127483547
|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; 2
|CLNHGVS=NC_000010.10:g.127483547C>A; NC_000010.10:g.127483547C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606938.0012; 606938.0010
|CLNSIG=5
|CLNCUI=C0162530
|CLNDBN=Congenital erythropoietic porphyria
|Disease=Congenital erythropoietic porphyria
|CLNACC=RCV000003959.2; RCV000003957.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK154652:C0162530:263700:79277
}}