{{Rsnum
|rsid=104894327
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=AICDA
|position=8604898
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AICDA
}}{{omim
|id=605257
|rsnum=104894327
|variant=0007
}}{{ClinVar
|rsid=104894327
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=8757494
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=AICDA:57379
|GENE_NAME=AICDA
|GENE_ID=57379
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.8757494A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605257.0007
|CLNSIG=5
|CLNCUI=C1720956
|CLNDBN=Immunodeficiency with hyper IgM type 2
|Disease=Immunodeficiency with hyper IgM type 2
|CLNACC=RCV000005435.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1720956:605258
}}