{{Rsnum
|rsid=137852649
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ACADSB
|position=123043127
|Gene_s=ACADSB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600301
|variant=0002
|rsnum=137852649
}}{{ClinVar
|rsid=137852649
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=124802643
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ACADSB:36
|GENE_NAME=ACADSB
|GENE_ID=36
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.124802643C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600301.0002
|CLNSIG=5
|CLNCUI=C1864912
|CLNDBN=Deficiency of 2-methylbutyryl-CoA dehydrogenase
|Disease=Deficiency of 2-methylbutyryl-CoA dehydrogenase
|CLNACC=RCV000009778.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1864912:610006:79157:444838008
}}