{{Rsnum
|rsid=147105770
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ERCC4
|position=13935697
|Gene_s=ERCC4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=16
|CLNACC=RCV000049250.26
|CLNALLE=1
|CLNDBN=XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME
|CLNDSDB=MedGen
|CLNDSDBID=CN177726
|CLNHGVS=NC_000016.9:g.14029554C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=133520.0010
|Disease=XERODERMA PIGMENTOSUM
|FwdALT=T
|FwdREF=C
|GENEINFO=ERCC4:2072
|GENE_ID=2072
|GENE_NAME=ERCC4
|REF=C
|RSPOS=14029554
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;VLD;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000040002100100
|WGT=0
|dbSNPBuildID=134
|rsid=147105770
}}