{{Rsnum
|rsid=58639322
|Gene=ACADSB
|Chromosome=10
|position=123040605
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ACADSB
}}{{omim
|id=600301
|rsnum=58639322
|variant=0004
}}{{ClinVar
|ALT=T
|CAF=0.9991; 0.0009183
|CHROM=10
|CLNACC=RCV000009780.3
|CLNALLE=1
|CLNDBN=Deficiency of 2-methylbutyryl-CoA dehydrogenase
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1864912:610006:79157:444838008
|CLNHGVS=NC_000010.10:g.124800121C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600301.0004
|COMMON=0
|Disease=Deficiency of 2-methylbutyryl-CoA dehydrogenase
|FwdALT=T
|FwdREF=C
|GENEINFO=ACADSB:36
|GENE_ID=36
|GENE_NAME=ACADSB
|REF=C
|RSPOS=124800121
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000040016110100
|WGT=0
|dbSNPBuildID=129
|rsid=58639322
}}