{{Rsnum
|rsid=121964998
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HMGCL
|position=23804441
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HMGCL
}}{{omim
|id=246450
|rsnum=121964998
|variant=0005
}}{{ClinVar
|rsid=121964998
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=23804441
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=HMGCL:3155
|GENE_NAME=HMGCL
|GENE_ID=3155
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.23804441C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000012736.1
|CLNDBN=Deficiency of hydroxymethylglutaryl-CoA lyase
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1134:C0268601:246450:ORPHA20:124611007
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_000191.2:c.835G>A; 613898.0005
|Disease=Deficiency of hydroxymethylglutaryl-CoA lyase
}}