{{Rsnum
|rsid=149724959
|Chromosome=9
|position=69035784
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=FXN
|Gene_s=FXN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=9
|CLNALLE=1
|CLNDBN=Friedreich ataxia 1
|CLNDSDB=OMIM
|CLNDSDBID=229300
|CLNHGVS=NC_000009.11:g.71650700delT
|CLNORIGIN=0
|CLNSIG=5
|Disease=Friedreich ataxia 1
|FwdREF=T
|GENEINFO=FXN:2395
|GENE_ID=2395
|GENE_NAME=FXN
|REF=AT
|RSPOS=71650699
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;NSF;REF;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168001201000002110200
|WGT=1
|dbSNPBuildID=134
|rsid=149724959
}}{{PMID Auto
|PMID=9150176
|Title=Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion.
|OA=1
}}

{{PMID Auto
|PMID=12112211
|Title=Friedreich's ataxia with chorea and myoclonus caused by a compound heterozygosity for a novel deletion and the trinucleotide GAA expansion.
}}