{{Rsnum
|rsid = 28934602
|Gene = HLCS
|geno1 = (G;G)
|geno2 = (G;T)
|geno3 = (T;T)
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=G
|Chromosome=21
|position=36936798
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HLCS
}}{{omim
|desc=HOLOCARBOXYLASE SYNTHETASE DEFICIENCY
|id=609018
|rsnum=28934602
|variant=0009
}}

{{ClinVar
|rsid=28934602
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=38309098
|CHROM=21
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=HLCS:3141
|GENE_NAME=HLCS
|GENE_ID=3141
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000021.8:g.38309098A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609018.0009
|CLNSIG=5
|CLNCUI=C0268581
|CLNDBN=Holocarboxylase synthetase deficiency
|Disease=Holocarboxylase synthetase deficiency
|CLNACC=RCV000001991.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0268581:253270:79242
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}