{{Rsnum
|rsid=137852769
|Gene=HADHA
|Chromosome=2
|position=26195184
|Orientation=plus
|GMAF=0.0
|Gene_s=HADHA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{omim
|id=600890
|variant=0001
|rsnum=137852769
}}{{ClinVar
|rsid=137852769
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=26418053
|CHROM=2
|GMAF=0
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=HADHA:3030
|GENE_NAME=HADHA
|GENE_ID=3030
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.26418053C>G
|CLNSRC=GTR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=GTR000246713; GTR000502755; 600890.0001
|CLNSIG=5
|CLNCUI=C0342786; CN069199
|CLNDBN=Mitochondrial trifunctional protein deficiency; Lchad deficiency with maternal acute fatty liver of pregnancy
|Disease=Mitochondrial trifunctional protein deficiency; Lchad deficiency with maternal acute fatty liver of pregnancy
|CLNACC=RCV000009266.1; RCV000009267.1
|Tags=RV;PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=1; 0
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=C0342786:609015:746:237999008; CN069199
|COMMON=0
}}