{{Rsnum
|rsid=137853326
|Chromosome=X
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=IKBKG
|position=154564451
|Gene_s=IKBKG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300248
|variant=0010
|rsnum=137853326
}}{{ClinVar
|rsid=137853326
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=153792666
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=IKBKG:8517
|GENE_NAME=IKBKG
|GENE_ID=8517
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000023.10:g.153792666G>A; NC_000023.10:g.153792666G>T
|CLNSRC=UniProtKB (variants); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=VAR_026496; 300248.0010; VAR_011325
|CLNSIG=5
|CLNCUI=C1846006
|CLNDBN=not provided; Hypohidrotic ectodermal dysplasia with immune deficiency
|Disease=not provided; Hypohidrotic ectodermal dysplasia with immune deficiency
|CLNACC=RCV000059067.1; RCV000012211.19; RCV000059068.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1846006:300291:238468:98813
}}{{PMID Auto
|PMID=11242109
|Title=X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling.
}}

{{PMID Auto
|PMID=15100680
|Title=The presentation and natural history of immunodeficiency caused by nuclear factor kappaB essential modulator mutation.
}}