{{Rsnum
|rsid=119470019
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GFM1
|position=158645686
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GFM1
}}{{omim
|id=606639
|rsnum=119470019
|variant=0002
}}{{ClinVar
|rsid=119470019
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=158363475
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GFM1:85476
|GENE_NAME=GFM1
|GENE_ID=85476
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.158363475C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606639.0002
|CLNSIG=5
|CLNCUI=C1836797
|CLNDBN=Combined oxidative phosphorylation deficiency 1
|Disease=Combined oxidative phosphorylation deficiency 1
|CLNACC=RCV000004378.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1836797:609060
}}