{{Rsnum
|rsid=118204106
|Chromosome=11
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=HMBS
|position=119089084
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HMBS
}}{{omim
|id=609806
|rsnum=118204106
|variant=0018
}}{{ClinVar
|rsid=118204106
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=118959794
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HMBS:3145
|GENE_NAME=HMBS
|GENE_ID=3145
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.118959794G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609806.0018
|CLNSIG=5
|CLNCUI=C0162565
|CLNDBN=Acute intermittent porphyria
|Disease=Acute intermittent porphyria
|CLNACC=RCV000001523.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1193:C0162565:176000:79276:234422006
}}