{{Rsnum
|rsid=193922574
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RAG2
|position=36593952
|Gene_s=RAG2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922574
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=36615502
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.36615502G>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Severe combined immunodeficiency disease
|Disease=Severe combined immunodeficiency disease
|Tags=RV;PM;PMC;OTHERKG;LSD
|CLNACC=RCV000030398.1
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0085110:31323000
|GENEINFO=RAG2:5897; C11orf74:119710
|GENE_ID=5897; 119710
|GENE_NAME=RAG2; C11orf74
}}{{PMID Auto
|PMID=20603253
|Title=Why newborn screening for severe combined immunodeficiency is essential: a case report.
}}