{{Rsnum
|rsid=104894421
|Chromosome=13
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LIG4
|position=108210436
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LIG4
}}{{omim
|id=601837
|rsnum=104894421
|variant=0004
}}{{ClinVar
|rsid=104894421
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=108862784
|CHROM=13
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=LIG4:3981
|GENE_NAME=LIG4
|GENE_ID=3981
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.108862784C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601837.0004
|CLNSIG=5
|CLNCUI=C1847827
|CLNDBN=Lig4 syndrome
|Disease=Lig4 syndrome
|CLNACC=RCV000008114.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1847827:606593:99812
}}