{{Rsnum
|rsid=35691292
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RAG2
|position=36593525
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=C11orf74,RAG2
}}{{omim
|id=179616
|rsnum=35691292
|variant=0007
}}

{{ population diversity
| geno1 = (C;C)
| geno2 = (C;T)
| geno3 = 
| CEU | 0 | 0 | 0
| HCB | 0 | 0 | 0
| JPT | 0 | 0 | 0
| YRI | 0 | 0 | 0
| ASW | 0 | 0 | 0
| CHD | 0 | 0 | 0
| GIH | 93.2 | 6.8 | 0
| LWK | 0 | 0 | 0
| MEX | 0 | 0 | 0
| MKK | 0 | 0 | 0
| TSI | 0 | 0 | 0
}}{{ClinVar
|rsid=35691292
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=36615075
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050160000000040503110100
|GENEINFO=RAG2:5897; C11orf74:119710
|GENE_NAME=RAG2; C11orf74
|GENE_ID=5897; 119710
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.36615075G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;SLO;VLD;HD;GNO;OTHERKG;PH3;LSD;OM
|CLNACC=RCV000014016.23
|CLNDBN=Severe combined immunodeficiency, b cell-negative
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=179616.0007
|Disease=Severe combined immunodeficiency
}}

{{on chip | Illumina Human 1M}}