{{Rsnum
|rsid=104894554
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=ATPAF2
|position=18028276
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATPAF2
}}{{omim
|id=608918
|rsnum=104894554
|variant=0001
}}{{ClinVar
|rsid=104894554
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=17931590
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ATPAF2:91647
|GENE_NAME=ATPAF2
|GENE_ID=91647
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.17931590A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608918.0001
|CLNSIG=5
|CLNCUI=C2700431
|CLNDBN=Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1
|Disease=Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1
|CLNACC=RCV000002072.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2700431:604273
}}