{{Rsnum
|rsid=120074171
|Gene=HGD
|Chromosome=3
|position=120638471
|Orientation=minus
|GMAF=0.0
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=HGD
}}{{omim
|id=607474
|rsnum=120074171
|variant=0007
}}{{ClinVar
|rsid=120074171
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=120357318
|CHROM=3
|GMAF=0
|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.120357318C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607474.0007
|CLNSIG=5
|CLNCUI=C0002066
|CLNDBN=Alkaptonuria
|Disease=Alkaptonuria
|CLNACC=RCV000003317.1
|Tags=RV;PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=1; 0
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1454:C0002066:203500:56
|COMMON=0
}}