{{Rsnum
|rsid=137853064
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYD88
|position=38140510
|Gene_s=MYD88
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=602170
|variant=0002
|rsnum=137853064
}}{{ClinVar
|rsid=137853064
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=38182001
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MYD88:4615
|GENE_NAME=MYD88
|GENE_ID=4615
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.38182001C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602170.0002
|CLNSIG=5
|CLNCUI=C2677092
|CLNDBN=Myd88 deficiency
|Disease=Myd88 deficiency
|CLNACC=RCV000007924.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2677092:612260:183713
}}