{{Rsnum
|rsid=121913664
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NFKBIA
|position=35404613
|Gene_s=NFKBIA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=164008
|rsnum=121913664
|variant=0002
}}{{ClinVar
|rsid=121913664
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=35873819
|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.35873819C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=164008.0002
|CLNSIG=5
|CLNCUI=C2677481
|CLNDBN=Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant
|Disease=Ectodermal dysplasia
|CLNACC=RCV000015041.24
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C2677481:612132:238468:98813
}}