{{Rsnum
|rsid=146948377
|Chromosome=9
|position=69065038
|Orientation=plus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=FXN
|Gene_s=FXN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=T
|CHROM=9
|CLNALLE=1
|CLNDBN=Friedreich ataxia 1
|CLNDSDB=OMIM
|CLNDSDBID=229300
|CLNHGVS=NC_000009.11:g.71679954delA
|CLNORIGIN=0
|CLNSIG=5
|Disease=Friedreich ataxia 1
|FwdREF=A
|GENEINFO=FXN:2395
|GENE_ID=2395
|GENE_NAME=FXN
|REF=TA
|RSPOS=71679953
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;NSF;REF;INT;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168081201000002110200
|WGT=1
|dbSNPBuildID=134
|rsid=146948377
}}{{PMID Auto
|PMID=9989622
|Title=Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
}}