{{Rsnum
|rsid = 28941774
|Gene = UROS
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=10
|position=125815081
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=UROS
}}{{omim
|desc=PORPHYRIA, CONGENITAL ERYTHROPOIETIC
|id=606938
|rsnum=28941774
|variant=0003
}}
{{ neighbor
| rsid = 28941775
| distance = 13
}}

{{ClinVar
|rsid=28941774
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=127503650
|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.127503650G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK154652; 606938.0003
|CLNSIG=5
|CLNCUI=C0162530
|CLNDBN=Congenital erythropoietic porphyria
|Disease=Congenital erythropoietic porphyria
|CLNACC=RCV000003950.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK154652:C0162530:263700:79277
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}