{{Rsnum
|rsid=104894322
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=AICDA
|position=8605227
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AICDA
}}{{omim
|id=605257
|rsnum=104894322
|variant=0005
}}{{ClinVar
|rsid=104894322
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=8757823
|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.8757823T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605257.0005
|CLNSIG=5
|CLNCUI=C1720956
|CLNDBN=Immunodeficiency with hyper IgM type 2
|Disease=Immunodeficiency with hyper IgM type 2
|CLNACC=RCV000005433.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1720956:605258
}}