{{Rsnum
|rsid=121912628
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RAD50
|position=132618182
|Gene_s=RAD50
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=604040
|rsnum=121912628
|variant=0001
}}{{ClinVar
|rsid=121912628
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=131953874
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RAD50:10111
|GENE_NAME=RAD50
|GENE_ID=10111
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.131953874C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604040.0001
|CLNSIG=5
|CLNCUI=C2751318
|CLNDBN=Nijmegen breakage syndrome-like disorder
|Disease=Nijmegen breakage syndrome-like disorder
|CLNACC=RCV000006230.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2751318:613078
}}