{{Rsnum
|rsid=111033539
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=UGT1A1
|position=233767160
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=UGT1A1,UGT1A3,UGT1A4,UGT1A5,UGT1A6,UGT1A7,UGT1A8,UGT1A9,UGT1A10
}}{{omim
|id=191740
|rsnum=111033539
|variant=0003
}}{{ClinVar
|rsid=111033539
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=234675806
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=UGT1A5:54579; UGT1A9:54600; UGT1A3:54659; UGT1A6:54578; UGT1A4:54657; UGT1A1:54658; UGT1A8:54576; UGT1A10:54575; UGT1A7:54577
|GENE_NAME=UGT1A5; UGT1A9; UGT1A3; UGT1A6; UGT1A4; UGT1A1; UGT1A8; UGT1A10; UGT1A7
|GENE_ID=54579; 54600; 54659; 54578; 54657; 54658; 54576; 54575; 54577
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.234675806C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=191740.0003
|CLNSIG=5
|CLNCUI=C0010324
|CLNDBN=Crigler Najjar syndrome, type 1
|Disease=Crigler Najjar syndrome
|CLNACC=RCV000013055.21
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C0010324:218800
}}