{{Rsnum
|rsid=104894419
|Gene=LIG4
|Chromosome=13
|position=108208829
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=LIG4
}}{{omim
|id=601837
|rsnum=104894419
|variant=0002
}}{{ClinVar
|rsid=104894419
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=108861177
|CHROM=13
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000016110100
|GENEINFO=LIG4:3981
|GENE_NAME=LIG4
|GENE_ID=3981
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.108861177G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601837.0002
|CLNSIG=5
|CLNCUI=C1847827
|CLNDBN=Lig4 syndrome
|Disease=Lig4 syndrome
|CLNACC=RCV000008112.1
|Tags=RV;PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1847827:606593:99812
|COMMON=0
}}
{{PMID Auto
|PMID=24892279
|Title=Dubowitz Syndrome Is a Complex Comprised of Multiple, Genetically Distinct and Phenotypically Overlapping Disorders
}}