{{Rsnum
|rsid=104894029
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=NT5C3
|position=33015741
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NT5C3A
}}{{omim
|id=606224
|rsnum=104894029
|variant=0010
}}{{ClinVar
|rsid=104894029
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=33055353
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NT5C3A:51251
|GENE_NAME=NT5C3A
|GENE_ID=51251
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.33055353C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606224.0010
|CLNSIG=5
|CLNCUI=C1849507
|CLNDBN=Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to
|Disease=Uridine 5-prime monophosphate hydrolase deficiency
|CLNACC=RCV000004745.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1849507:266120:35120
}}