{{Rsnum
|rsid=104894562
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FOXN1
|position=28529157
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FOXN1
}}{{omim
|id=600838
|rsnum=104894562
|variant=0001
}}{{ClinVar
|rsid=104894562
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=26856175
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FOXN1:8456
|GENE_NAME=FOXN1
|GENE_ID=8456
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.26856175C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600838.0001
|CLNSIG=5
|CLNCUI=C1866426
|CLNDBN=T-cell immunodeficiency, congenital alopecia and nail dystrophy
|Disease=T-cell immunodeficiency
|CLNACC=RCV000009300.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1866426:601705:169095
}}