{{Rsnum
|rsid=193922347
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=IL2RG
|position=71110644
|Gene_s=IL2RG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922347
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=70330494
|CHROM=X
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.70330494T>C
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=X-linked severe combined immunodeficiency
|Disease=X-linked severe combined immunodeficiency
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000030054.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1410:C1279481:300400:276:203592006
|GENEINFO=IL2RG:3561
|GENE_ID=3561
|GENE_NAME=IL2RG
}}{{PMID Auto
|PMID=8961626
|Title=IL2RGbase: a database of gamma c-chain defects causing human X-SCID.
}}

{{PMID Auto
|PMID=10444186
|Title=Identification of X-linked severe combined immunodeficiency by mutation analysis of blood and hair roots.
}}