{{Rsnum
|rsid=387907213
|Chromosome=8
|position=116847643
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RAD21
|Gene_s=RAD21
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=8
|CLNACC=RCV000029139.1
|CLNALLE=1
|CLNDBN=Cornelia de Lange syndrome 4
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1104:CN130277:614701:199
|CLNHGVS=NC_000008.10:g.117859882A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606462.0002
|Disease=Cornelia de Lange syndrome 4
|FwdALT=C
|FwdREF=T
|REF=A
|RSPOS=117859882
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907213
|GENEINFO=RAD21:5885
|GENE_ID=5885
|GENE_NAME=RAD21
}}