{{Rsnum
|rsid=121912629
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=RAD50
|position=132642364
|Gene_s=RAD50
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121912629
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=131978056
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=RAD50:10111
|GENE_NAME=RAD50
|GENE_ID=10111
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.131978056A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604040.0002
|CLNSIG=5
|CLNCUI=C2751318
|CLNDBN=Nijmegen breakage syndrome-like disorder
|Disease=Nijmegen breakage syndrome-like disorder
|CLNACC=RCV000006231.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2751318:613078
}}