{{Rsnum
|rsid=145854903
|Chromosome=9
|position=69035900
|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.71650816C>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=71650816
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;NSM;REF;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000a01000002110100
|WGT=1
|dbSNPBuildID=134
|rsid=145854903
}}{{PMID Auto
|PMID=15936968
|Title=Molecular and functional characterization of a human frataxin mutation found in hypertrophic cardiomyopathy.
}}