{{Rsnum
|rsid=111033540
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=UGT1A1
|position=233768333
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=UGT1A1,UGT1A3,UGT1A4,UGT1A5,UGT1A6,UGT1A7,UGT1A8,UGT1A9,UGT1A10
|Status=Merged
|Merged=28934877
}}{{omim
|id=191740
|rsnum=111033540
|variant=0022
}}{{ClinVar
|rsid=111033540
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=234676979
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=050260000a11000402110100
|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=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.234676979A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=191740.0022; 191740.0022
|CLNSIG=5
|CLNCUI=C0268311; C0017551
|CLNDBN=Crigler-Najjar syndrome, type II; Gilbert's syndrome
|Disease=Crigler-Najjar syndrome; Gilbert's syndrome
|CLNACC=SCV000033325.1; SCV000033326.1
|Tags=PM;S3D;NSM;REF;OTH;HD;OTHERKG;LSD;OM
}}