{{Rsnum
|rsid=1800556
|Gene=ACADS
|Chromosome=12
|position=120737875
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.02479
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ACADS
}}{{Venter SNP
|rsid=1800556
|allele=T
|frequency=
|uid=1103649554437
|type=heterozygous_SNP
|hugo=ACADS
|ensembl gene=ENSG00000122971
|ensembl transcript=ENST00000242592
|sift=AFFECT FUNCTION
|disease=Defects in ACADS are the cause of short-chain acyl-CoA dehydrogenase deficiency (SCAD deficiency) (MIM:201470). It is an autosomal recessive disorder resulting in acute acidosis and muscle weakness in infants, and a form of lipid-storage myopathy in adults.
}}

{{ neighbor
| rsid = 28940874
| distance = 64
}}

{{ neighbor
| rsid = 28940873
| distance = 1
}}

{{omim
|id=606885
|rsnum=1800556
|variant=0006
}}

{{ClinVar
|rsid=1800556
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=121175678
|CHROM=12
|GMAF=0.0252
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050368000000140516110100
|GENEINFO=ACADS:35
|GENE_NAME=ACADS
|GENE_ID=35
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.121175678C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606885.0006
|CLNSIG=5
|CLNCUI=C0342783
|CLNDBN=Deficiency of butyryl-CoA dehydrogenase
|Disease=Deficiency of butyryl-CoA dehydrogenase
|CLNACC=RCV000004034.1
|Tags=PM;PMC;S3D;SLO;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9752; 0.02479
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK63582:C0342783:201470:26792:124166007
|COMMON=1
}}

{{PMID|18704161|OA=1
}} Genetic variation in an individual human exome.

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