{{Rsnum
|rsid=118204105
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HMBS
|position=119088647
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HMBS
}}{{omim
|id=609806
|rsnum=118204105
|variant=0017
}}{{ClinVar
|rsid=118204105
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=118959357
|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.118959357C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609806.0017
|CLNSIG=5
|CLNCUI=C0162565
|CLNDBN=Acute intermittent porphyria
|Disease=Acute intermittent porphyria
|CLNACC=RCV000001520.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1193:C0162565:176000:79276:234422006
}}