{{Rsnum
|rsid=137853184
|Chromosome=8
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=C8orf38
|position=95032093
|Gene_s=C8orf38
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=612392
|variant=0001
|rsnum=137853184
}}{{ClinVar
|rsid=137853184
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=96044321
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=NDUFAF6:137682
|GENE_NAME=NDUFAF6
|GENE_ID=137682
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.96044321A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612392.0001
|CLNSIG=5
|CLNCUI=C1838951
|CLNDBN=Leigh syndrome due to mitochondrial complex I deficiency
|Disease=Leigh syndrome due to mitochondrial complex I deficiency
|CLNACC=RCV000000577.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1838951
}}