{{Rsnum
|rsid=1799958
|Gene=ACADS
|Chromosome=12
|position=120738280
|Orientation=plus
|GMAF=0.1763
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ACADS
}}{{omim
|id=606885
|rsnum=1799958
|variant=0007
}}

{{ClinVar
|rsid=1799958
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=121176083
|CHROM=12
|GMAF=0.1767
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050368000000150516110100
|GENEINFO=ACADS:35
|GENE_NAME=ACADS
|GENE_ID=35
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.121176083G>A
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=8601; 606885.0007
|CLNSIG=5
|CLNCUI=C0342783
|CLNDBN=Deficiency of butyryl-CoA dehydrogenase; AllHighlyPenetrant
|Disease=Deficiency of butyryl-CoA dehydrogenase; AllHighlyPenetrant
|CLNACC=RCV000004035.1; RCV000077896.1
|Tags=PM;PMC;S3D;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.8237; 0.1763
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK63582:C0342783:201470:26792:124166007; CN169374
|COMMON=1
}}

{{PMID Auto
|PMID=19470168
|Title=NPAS2 and PER2 are linked to risk factors of the metabolic syndrome.
|OA=1
}}

{{PMID Auto
|PMID=20180986
|Title=CLOCK is suggested to associate with comorbid alcohol use and depressive disorders.
|OA=1
}}

{{GET Evidence
|gene=ACADS
|aa_change=Gly209Ser
|aa_change_short=G209S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1799958
|overall_frequency_n=2087
|overall_frequency_d=10758
|overall_frequency=0.193995
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=21
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.993
|genetests_testable=Y
|nblosum100=2
|autoscore=3
|n_web_uneval=3
}}

{{on chip | HumanOmni1Quad}}