{{Rsnum
|rsid=137852772
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HADHA
|position=26209840
|Gene_s=HADHA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600890
|variant=0007
|rsnum=137852772
}}{{ClinVar
|rsid=137852772
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=26432709
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HADHA:3030
|GENE_NAME=HADHA
|GENE_ID=3030
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.26432709A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600890.0007
|CLNSIG=5
|CLNCUI=C0342786
|CLNDBN=Mitochondrial trifunctional protein deficiency
|Disease=Mitochondrial trifunctional protein deficiency
|CLNACC=RCV000009273.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0342786:609015:746:237999008
}}