{{Rsnum
|rsid=387907094
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TTC19
|position=16003885
|Gene_s=TTC19
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=17
|CLNACC=RCV000024068.3
|CLNALLE=1
|CLNDBN=Mitochondrial complex III deficiency, nuclear type 2
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN169526:615157
|CLNHGVS=NC_000017.10:g.15907199C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613814.0002
|Disease=Mitochondrial complex III deficiency
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=15907199
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907094
|GENEINFO=TTC19:54902
|GENE_ID=54902
|GENE_NAME=TTC19
}}