{{Rsnum
|rsid=34557412
|Gene=TNFRSF13B
|Chromosome=17
|position=16948873
|Orientation=plus
|GMAF=0.003214
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TNFRSF13B
}}{{omim
|id=604907
|rsnum=34557412
|variant=0001
}}

{{ClinVar
|rsid=34557412
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=16852187
|CHROM=17
|GMAF=0.0032
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050360000000040116110100
|GENEINFO=TNFRSF13B:23495
|GENE_NAME=TNFRSF13B
|GENE_ID=23495
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.16852187A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604907.0001
|CLNSIG=5
|CLNCUI=C0009447; C1836032
|CLNDBN=Common variable agammaglobulinemia; Immunoglobulin A deficiency 2
|Disease=Common variable agammaglobulinemia; Immunoglobulin A deficiency 2
|CLNACC=RCV000005623.1; RCV000005624.1
|Tags=RV;PM;S3D;SLO;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9968; 0.003214
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM
|CLNDSDBID=NBK1299:C0009447:240500:1572:23238000; C1836032:609529
|COMMON=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}