{{Rsnum
|rsid=193922641
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=IL7R
|position=35867437
|Gene_s=IL7R
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922641
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=35867539
|CHROM=5
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.35867539G>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Severe combined immunodeficiency disease
|Disease=Severe combined immunodeficiency disease
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000030061.1
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0085110:31323000
|GENEINFO=IL7R:3575
|GENE_ID=3575
|GENE_NAME=IL7R
}}{{PMID|18255|OA=1
}} New technique for the treatment of endstage renal failure.

{{PMID|15661025}} Interleukin-7 receptor alpha (IL-7Ralpha) deficiency: cellular and molecular bases. Analysis of clinical, immunological, and molecular features in 16 novel patients.

{{PMID|16492442}} Omenn syndrome in an infant with IL7RA gene mutation.

{{PMID|17827065|OA=1
}} IL-7 receptor deficient SCID with a unique intronic mutation and post-transplant autoimmunity due to chronic GVHD.

{{PMID|18403192}} Genetically determined lymphopenia and autoimmune manifestations.

{{PMID|18641513}} Mutations causing severe combined immunodeficiency: detection with a custom resequencing microarray.