{{Rsnum
|rsid=104893894
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=IL7R
|position=35871070
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=IL7R
}}{{omim
|id=146661
|rsnum=104893894
|variant=0005
}}{{ClinVar
|rsid=104893894
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=35871172
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=IL7R:3575
|GENE_NAME=IL7R
|GENE_ID=3575
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.35871172C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=146661.0005
|CLNSIG=5
|CLNCUI=C1837028
|CLNDBN=Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive
|Disease=Severe combined immunodeficiency
|CLNACC=RCV000015968.20
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1837028:608971
}}