{{Rsnum
|rsid=121434323
|Chromosome=5
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=ERCC8
|position=60890964
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ERCC8
}}{{omim
|id=609412
|rsnum=121434323
|variant=0002
}}{{ClinVar
|rsid=121434323
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=60186791
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ERCC8:1161
|GENE_NAME=ERCC8
|GENE_ID=1161
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.60186791G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609412.0002
|CLNSIG=5
|CLNCUI=C0751039
|CLNDBN=Cockayne syndrome type A
|Disease=Cockayne syndrome type A
|CLNACC=RCV000001785.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1342:C0751039:216400:191:21086008
}}