{{Rsnum
|rsid=119103229
|Chromosome=21
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HLCS
|position=36765170
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HLCS
}}{{omim
|id=609018
|rsnum=119103229
|variant=0004
}}{{ClinVar
|rsid=119103229
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=38137471
|CHROM=21
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HLCS:3141
|GENE_NAME=HLCS
|GENE_ID=3141
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000021.8:g.38137471G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609018.0004
|CLNSIG=5
|CLNCUI=C0268581
|CLNDBN=Holocarboxylase synthetase deficiency
|Disease=Holocarboxylase synthetase deficiency
|CLNACC=RCV000001986.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0268581:253270:79242
}}