{{Rsnum
|rsid=121909485
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TSFM
|position=57796539
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AVIL,TSFM
}}{{omim
|id=604723
|rsnum=121909485
|variant=0001
}}{{ClinVar
|rsid=121909485
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=58190322
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TSFM:10102
|GENE_NAME=TSFM
|GENE_ID=10102
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.58190322C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604723.0001
|CLNSIG=5
|CLNCUI=C1864840
|CLNDBN=Combined oxidative phosphorylation deficiency 3
|Disease=Combined oxidative phosphorylation deficiency 3
|CLNACC=RCV000005710.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1864840:610505:168566
}}