{{Rsnum
|rsid=121908012
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=UROS
|position=125815061
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=UROS
}}{{omim
|id=606938
|rsnum=121908012
|variant=0001
}}{{ClinVar
|rsid=121908012
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=127503630
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000040002110100
|GENEINFO=UROS:7390
|GENE_NAME=UROS
|GENE_ID=7390
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.127503630A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK154652; 606938.0001
|CLNSIG=5
|CLNCUI=C0162530
|CLNDBN=Congenital erythropoietic porphyria
|Disease=Congenital erythropoietic porphyria
|CLNACC=RCV000003948.2
|Tags=RV;PM;S3D;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK154652:C0162530:263700:79277
}}