{{Rsnum
|rsid=104894380
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=UNG
|position=109103562
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=UNG
}}{{omim
|id=191525
|rsnum=104894380
|variant=0003
}}{{ClinVar
|rsid=104894380
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=109541367
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=UNG:7374
|GENE_NAME=UNG
|GENE_ID=7374
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.109541367T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=191525.0003
|CLNSIG=5
|CLNCUI=C1720958
|CLNDBN=Immunodeficiency with hyper IgM type 5
|Disease=Immunodeficiency with hyper IgM type 5
|CLNACC=RCV000013086.23
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1720958:608106
}}