{{Rsnum
|rsid = 28935475
|Gene = HSD17B10
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=X
|position=53432086
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HSD17B10
}}{{omim
|desc=2-@METHYL-3-HYDROXYBUTYRYL-CoA DEHYDROGENASE DEFICIENCY
|id=300256
|rsnum=28935475
|variant=0001
}}
{{ neighbor
| rsid = 28935476
| distance = 24
}}

{{ClinVar
|rsid=28935475
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=53459034
|CHROM=X
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050268000000000402110100
|GENEINFO=HSD17B10:3028
|GENE_NAME=HSD17B10
|GENE_ID=3028
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.53459034G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300256.0001
|CLNSIG=5
|CLNCUI=C1845517
|CLNDBN=2-methyl-3-hydroxybutyric aciduria
|Disease=2-methyl-3-hydroxybutyric aciduria
|CLNACC=RCV000012195.10
|Tags=RV;PM;PMC;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1845517:300438
}}

{{PMID Auto
|PMID=19706438
|Title=Mental retardation linked to mutations in the HSD17B10 gene interfering with neurosteroid and isoleucine metabolism.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}