{{Rsnum
|rsid=121913016
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ERCC2
|position=45357368
|Gene_s=ERCC2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=126340
|rsnum=121913016
|variant=0001
}}{{ClinVar
|rsid=121913016
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=45860626
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000040002110100
|GENEINFO=ERCC2:2068
|GENE_NAME=ERCC2
|GENE_ID=2068
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.45860626G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=126340.0001
|CLNSIG=5
|CLNCUI=C0268138; C0740342
|CLNDBN=Xeroderma pigmentosum, group D; BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome
|Disease=Xeroderma pigmentosum; BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome
|CLNACC=RCV000018267.22; RCV000018268.26
|Tags=RV;PM;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT; MedGen:SNOMED_CT
|CLNDSDBID=NBK1397:C0268138:278730:68637004; C0740342:403796005
}}