{{Rsnum
|rsid=122462164
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HSD17B10
|position=53431819
|Gene_s=HSD17B10
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300256
|variant=0004
|rsnum=122462164
}}{{ClinVar
|rsid=122462164
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=53458767
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HSD17B10:3028
|GENE_NAME=HSD17B10
|GENE_ID=3028
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.53458767G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300256.0004
|CLNSIG=5
|CLNCUI=C1846168
|CLNDBN=Mental retardation, X-linked, syndromic 10
|Disease=Mental retardation
|CLNACC=RCV000012198.10
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1846168:300220:85295
}}