{{Rsnum
|rsid=137854888
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=DNAJC19
|position=180987023
|Gene_s=DNAJC19
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=608977
|variant=0001
|rsnum=137854888
}}{{ClinVar
|rsid=137854888
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=180704811
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=0
|VP=0x050068000000000002110100
|GENEINFO=DNAJC19:131118
|GENE_NAME=DNAJC19
|GENE_ID=131118
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.180704811C>G
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608977.0001
|CLNSIG=5
|CLNCUI=C1857776
|CLNDBN=3-methylglutaconic aciduria type V
|Disease=3-methylglutaconic aciduria type V
|CLNACC=RCV000002028.1
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1857776:610198:66634
}}{{PMID Auto
|PMID=16055927
|Title=Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition.
|OA=1
}}