{{Rsnum
|rsid=121917902
|Chromosome=10
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PGBD3
|position=49524073
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ERCC6,PGBD3
}}{{omim
|id=609413
|rsnum=121917902
|variant=0004
}}{{ClinVar
|rsid=121917902
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=50732119
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ERCC6-PGBD3:101243544; ERCC6:2074; PGBD3:267004
|GENE_NAME=ERCC6-PGBD3; ERCC6; PGBD3
|GENE_ID=101243544; 2074; 267004
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.50732119G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609413.0004
|CLNSIG=5
|CLNCUI=C0751038
|CLNDBN=Cockayne syndrome, type B
|Disease=Cockayne syndrome
|CLNACC=RCV000001772.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1342:C0751038:133540:191
}}