{{Rsnum
|rsid=397518435
|Chromosome=7
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=NT5C3A
|position=33015871
|Gene_s=NT5C3A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,G
|CHROM=7
|CLNACC=RCV000004738.2; RCV000004742.2
|CLNALLE=1; 2
|CLNDBN=Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1849507:266120:35120
|CLNHGVS=NC_000007.13:g.33055483C>A; NC_000007.13:g.33055483C>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606224.0003; 606224.0007
|Disease=Uridine 5-prime monophosphate hydrolase deficiency
|FwdALT=C,T
|FwdREF=G
|GENEINFO=NT5C3A:51251
|GENE_ID=51251
|GENE_NAME=NT5C3A
|REF=C
|RSPOS=33055483
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=397518435
}}