{{Rsnum
|rsid = 28933100
|Gene = NFKBIA
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=T
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=14
|position=35404550
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NFKBIA
}}{{omim
|desc=ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT
|id=164008
|rsnum=28933100
|variant=0001
}}

{{ClinVar
|rsid=28933100
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=35873756
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=NFKBIA:4792
|GENE_NAME=NFKBIA
|GENE_ID=4792
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.35873756C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=164008.0001
|CLNSIG=5
|CLNCUI=C2677481
|CLNDBN=Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant
|Disease=Ectodermal dysplasia
|CLNACC=RCV000015040.24
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C2677481:612132:238468:98813
}}

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