{{Rsnum
|rsid=72553883
|Gene=TNFRSF13B
|Chromosome=17
|position=16940415
|Orientation=plus
|GMAF=0.003673
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=TNFRSF13B
}}{{omim
|id=604907
|rsnum=72553883
|variant=0002
}}

{{ClinVar
|rsid=72553883
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=16843729
|CHROM=17
|GMAF=0.0037
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050060000000040416110100
|GENEINFO=TNFRSF13B:23495
|GENE_NAME=TNFRSF13B
|GENE_ID=23495
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.16843729G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604907.0002
|CLNSIG=5
|CLNCUI=C0009447; C1836032
|CLNDBN=Common variable agammaglobulinemia; Immunoglobulin A deficiency 2
|Disease=Common variable agammaglobulinemia; Immunoglobulin A deficiency 2
|CLNACC=RCV000005625.1; RCV000005626.1
|Tags=RV;PM;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9963; 0.003673
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM
|CLNDSDBID=NBK1299:C0009447:240500:1572:23238000; C1836032:609529
|COMMON=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}