{{Rsnum
|rsid=57443665
|Gene=ACADS
|Chromosome=12
|position=120737893
|Orientation=plus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=ACADS
}}{{omim
|id=606885
|rsnum=57443665
|variant=0004
}}{{ClinVar
|rsid=57443665
|Reversed=0
|FwdREF=T
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=121175696
|CHROM=12
|GMAF=0.0014
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000040416110100
|GENEINFO=ACADS:35
|GENE_NAME=ACADS
|GENE_ID=35
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.121175696T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606885.0004
|CLNSIG=5
|CLNCUI=C0342783
|CLNDBN=Deficiency of butyryl-CoA dehydrogenase
|Disease=Deficiency of butyryl-CoA dehydrogenase
|CLNACC=RCV000004032.1
|Tags=PM;S3D;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377; .
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK63582:C0342783:201470:26792:124166007
|COMMON=0
}}{{GET Evidence
|gene=ACADS
|aa_change=Trp177Arg
|aa_change_short=W177R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs57443665
|overall_frequency_n=24
|overall_frequency_d=10758
|overall_frequency=0.0022309
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.996
|genetests_testable=Y
|nblosum100=7
|autoscore=4
|n_web_uneval=1
}}