{{Rsnum
|rsid=119470018
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GFM1
|position=158646896
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GFM1
}}{{omim
|id=606639
|rsnum=119470018
|variant=0001
}}{{ClinVar
|rsid=119470018
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=158364685
|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.158364685A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606639.0001
|CLNSIG=5
|CLNCUI=C1836797
|CLNDBN=Combined oxidative phosphorylation deficiency 1
|Disease=Combined oxidative phosphorylation deficiency 1
|CLNACC=RCV000004377.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1836797:609060
}}