{{Rsnum
|rsid=25640
|Gene=HSD17B4
|Chromosome=5
|position=119475838
|Orientation=plus
|GMAF=0.3994
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=HSD17B4
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 22.1 | 50.4 | 27.4
| HCB | 25.9 | 53.3 | 20.7
| JPT | 15.2 | 60.7 | 24.1
| YRI | 0.7 | 14.3 | 85.0
| ASW | 5.4 | 37.5 | 57.1
| CHB | 25.9 | 53.3 | 20.7
| CHD | 33.3 | 47.2 | 19.4
| GIH | 19.8 | 44.6 | 35.6
| LWK | 1.8 | 20.2 | 78.0
| MEX | 27.6 | 53.4 | 19.0
| MKK | 0.0 | 11.0 | 89.0
| TSI | 23.8 | 41.6 | 34.7
| HapMapRevision=28
}}{{omim
|id=601860
|rsnum=25640
|variant=0005
}}

{{ClinVar
|rsid=25640
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=118811533
|CHROM=5
|GMAF=0.3993
|dbSNPBuildID=72
|SSR=0
|SAO=1
|VP=0x050360000000150517110101
|GENEINFO=HSD17B4:3295
|GENE_NAME=HSD17B4
|GENE_ID=3295
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000005.9:g.118811533G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601860.0005
|CLNSIG=5
|CLNCUI=C0342870
|CLNDBN=Bifunctional peroxisomal enzyme deficiency
|Disease=Bifunctional peroxisomal enzyme deficiency
|CLNACC=RCV000008096.1
|Tags=PM;S3D;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.6006; 0.3994; .
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0342870:261515:238068007
|COMMON=1
}}

{{GET Evidence
|gene=HSD17B4
|aa_change=Arg106His
|aa_change_short=R106H
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs25640
|overall_frequency_n=3894
|overall_frequency_d=10752
|overall_frequency=0.362165
|n_genomes=28
|n_genomes_annotated=0
|n_haplomes=35
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.547
|genetests_testable=Y
|nblosum100=1
|autoscore=2
|n_web_uneval=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}