{{Rsnum
|rsid=121908016
|Gene=UROS
|Chromosome=10
|position=125815034
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=UROS
}}{{omim
|id=606938
|rsnum=121908016
|variant=0009
}}{{ClinVar
|rsid=121908016
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=127503603
|CHROM=10
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000016110100
|GENEINFO=UROS:7390
|GENE_NAME=UROS
|GENE_ID=7390
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.127503603C>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK154652; 606938.0009
|CLNSIG=5
|CLNCUI=C0162530
|CLNDBN=Congenital erythropoietic porphyria
|Disease=Congenital erythropoietic porphyria
|CLNACC=RCV000003956.2
|Tags=RV;PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK154652:C0162530:263700:79277
|COMMON=0
}}