{{Rsnum
|rsid=137853327
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=IKBKG
|position=154564418
|Gene_s=IKBKG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300248
|variant=0011
|rsnum=137853327
}}{{ClinVar
|rsid=137853327
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=153792633
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=IKBKG:8517
|GENE_NAME=IKBKG
|GENE_ID=8517
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153792633A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300248.0011
|CLNSIG=5
|CLNCUI=C1846006
|CLNDBN=HYPER-IgM IMMUNODEFICIENCY, X-LINKED, WITH HYPOHIDROTIC ECTODERMAL DYSPLASIA; Hypohidrotic ectodermal dysplasia with immune deficiency
|Disease=HYPER-IgM IMMUNODEFICIENCY; Hypohidrotic ectodermal dysplasia with immune deficiency
|CLNACC=RCV000012212.1; RCV000024285.10
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1846006:300291:238468:98813
}}