{{Rsnum
|rsid=145045861
|Chromosome=9
|position=69053193
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=FXN
|Gene_s=FXN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=C
|CHROM=9
|CLNALLE=1
|CLNDBN=Friedreich ataxia 1
|CLNDSDB=OMIM
|CLNDSDBID=229300
|CLNHGVS=NC_000009.11:g.71668109delT
|CLNORIGIN=0
|CLNSIG=5
|Disease=Friedreich ataxia 1
|FwdREF=T
|GENEINFO=FXN:2395
|GENE_ID=2395
|GENE_NAME=FXN
|REF=CT
|RSPOS=71668106
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;SLO;NSF;REF;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050368001201000002110200
|WGT=1
|dbSNPBuildID=134
|rsid=145045861
}}{{PMID Auto
|PMID=10633132
|Title=Prevalence of mitochondrial gene mutations among hearing impaired patients.
|OA=1
}}