{{Rsnum
|rsid=137852508
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=IL2RG
|position=71108336
|Gene_s=IL2RG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=308380
|variant=0002
|rsnum=137852508
}}{{ClinVar
|rsid=137852508
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=70328186
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=CXorf65:158830; IL2RG:3561
|GENE_NAME=CXorf65; IL2RG
|GENE_ID=158830; 3561
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.70328186G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=308380.0002
|CLNSIG=5
|CLNCUI=C1279481
|CLNDBN=X-linked severe combined immunodeficiency
|Disease=X-linked severe combined immunodeficiency
|CLNACC=RCV000030058.1
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1410:C1279481:300400:276:203592006
}}{{PMID Auto
|PMID=7557965
|Title=Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2R gamma chain gene by single-strand conformation polymorphism analysis.
}}

{{PMID Auto
|PMID=8027558
|Title=Impairment of ligand binding and growth signaling of mutant IL-2 receptor gamma-chains in patients with X-linked severe combined immunodeficiency.
}}

{{PMID Auto
|PMID=8462096
|Title=Interleukin-2 receptor gamma chain mutation results in X-linked severe combined immunodeficiency in humans.
}}

{{PMID Auto
|PMID=8961626
|Title=IL2RGbase: a database of gamma c-chain defects causing human X-SCID.
}}

{{PMID Auto
|PMID=10784449
|Title=Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease.
}}

{{PMID Auto
|PMID=11961146
|Title=Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy.
}}