{{Rsnum
|rsid=121908379
|Chromosome=17
|Orientation=minus
|geno1=(CC;CC)
|geno2=(CC;GG)
|geno3=(GG;GG)
|Gene=TNFRSF13B
|position=16940375
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNFRSF13B
}}{{omim
|id=604907
|rsnum=121908379
|variant=0005
}}{{ClinVar
|rsid=121908379
|Reversed=1
|FwdREF=CC
|FwdALT=GG
|REF=AGG
|ALT=ACC
|RSPOS=16843688
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110800
|GENEINFO=TNFRSF13B:23495
|GENE_NAME=TNFRSF13B
|GENE_ID=23495
|WGT=0
|VC=MNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.16843689_16843690delGGinsCC
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604907.0005
|CLNSIG=5
|CLNCUI=C0009447
|CLNDBN=Common variable agammaglobulinemia
|Disease=Common variable agammaglobulinemia
|CLNACC=RCV000005630.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1299:C0009447:240500:1572:23238000
}}