{{Rsnum
|rsid=121913131
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HADHB
|position=26279292
|Gene_s=HADHB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=143450
|rsnum=121913131
|variant=0001
}}{{ClinVar
|rsid=121913131
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=26502160
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HADHB:3032
|GENE_NAME=HADHB
|GENE_ID=3032
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.26502160A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=143450.0001
|CLNSIG=5
|CLNCUI=C0342786
|CLNDBN=Mitochondrial trifunctional protein deficiency
|Disease=Mitochondrial trifunctional protein deficiency
|CLNACC=RCV000015969.20
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0342786:609015:746:237999008
}}