{{Rsnum
|rsid=149284013
|Chromosome=9
|position=69053173
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=FXN
|Gene_s=FXN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=AT
|CHROM=9
|CLNALLE=1
|CLNDBN=Friedreich ataxia 1
|CLNDSDB=OMIM
|CLNDSDBID=229300
|CLNHGVS=NC_000009.11:g.71668089_71668090insT
|CLNORIGIN=0
|CLNSIG=5
|Disease=Friedreich ataxia 1
|FwdALT=T
|GENEINFO=FXN:2395
|GENE_ID=2395
|GENE_NAME=FXN
|REF=A
|RSPOS=71668089
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;NSF;REF;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050368001201000002110200
|WGT=1
|dbSNPBuildID=134
|rsid=149284013
}}{{PMID Auto
|PMID=10982187
|Title=Genotype and phenotype analysis of Friedreich's ataxia compound heterozygous patients.
}}