{{Rsnum
|rsid=104894291
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RAG1
|position=36574491
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RAG1
}}{{omim
|id=179615
|rsnum=104894291
|variant=0008
}}{{ClinVar
|rsid=104894291
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=36596041
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=RAG1:5896
|GENE_NAME=RAG1
|GENE_ID=5896
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.36596041G>A; NC_000011.9:g.36596041G>T
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=179615.0008; VAR_025972
|CLNSIG=5
|CLNCUI=C1801959
|CLNDBN=Histiocytic medullary reticulosis; not provided
|Disease=Histiocytic medullary reticulosis; not provided
|CLNACC=RCV000014028.23; RCV000059557.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1801959:603554:39041:307650006
}}{{PMID|11133745}} V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations.