{{Rsnum
|rsid=121917900
|Chromosome=10
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ERCC6
|position=49500673
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ERCC6
}}{{omim
|id=609413
|rsnum=121917900
|variant=0001
}}{{ClinVar
|rsid=121917900
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=50708719
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ERCC6:2074
|GENE_NAME=ERCC6
|GENE_ID=2074
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.50708719C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609413.0001
|CLNSIG=5
|CLNCUI=C0751038
|CLNDBN=Cockayne syndrome, type B
|Disease=Cockayne syndrome
|CLNACC=RCV000001768.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1342:C0751038:133540:191
}}