{{Rsnum
|rsid=120074173
|Gene=HGD
|Chromosome=3
|position=120633233
|Orientation=minus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=HGD
}}{{omim
|id=607474
|rsnum=120074173
|variant=0009
}}{{ClinVar
|rsid=120074173
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=120352080
|CHROM=3
|GMAF=0.0009
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000016110100
|GENEINFO=HGD:3081
|GENE_NAME=HGD
|GENE_ID=3081
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.120352080T>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1454; 607474.0009
|CLNSIG=5
|CLNCUI=C0002066
|CLNDBN=Alkaptonuria
|Disease=Alkaptonuria
|CLNACC=RCV000003323.2
|Tags=RV;PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1454:C0002066:203500:56
|COMMON=0
}}