{{Rsnum
|rsid=193922461
|Chromosome=11
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=RAG1
|position=36574870
|Gene_s=RAG1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922461
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=36596420
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.36596420G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Combined cellular and humoral immune defects with granulomas; Histiocytic medullary reticulosis
|Disease=Combined cellular and humoral immune defects with granulomas; Histiocytic medullary reticulosis
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000022745.17; RCV000030389.1
|CLNDSDB=MedGen:OMIM; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C2673536:233650; C1801959:603554:39041:307650006
|CLNSRCID=179615.0024
|GENEINFO=RAG1:5896
|GENE_ID=5896
|GENE_NAME=RAG1
}}{{PMID Auto
|PMID=10701853
|Title=Prenatal diagnosis of RAG-deficient Omenn syndrome.
}}

{{PMID Auto
|PMID=20489056
|Title=Hypomorphic Rag mutations can cause destructive midline granulomatous disease.
|OA=1
}}

{{PMID Auto
|PMID=21131235
|Title=Analysis of mutations and recombination activity in RAG-deficient patients.
}}