{{Rsnum
|rsid=138034837
|Chromosome=9
|position=69072622
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|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.71687538C>T
|CLNORIGIN=0
|CLNSIG=5
|Disease=Friedreich ataxia 1
|FwdALT=T
|FwdREF=C
|GENEINFO=FXN:2395
|GENE_ID=2395
|GENE_NAME=FXN
|REF=C
|RSPOS=71687538
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;NSM;REF;SYN;INT;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368080b01000002110100
|WGT=1
|dbSNPBuildID=134
|rsid=138034837
}}{{PMID Auto
|PMID=10732799
|Title=The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.
}}

{{PMID Auto
|PMID=10766903
|Title=Frataxin point mutations in two patients with Friedreich's ataxia and unusual clinical features.
|OA=1
}}