{{Rsnum
|rsid=146818694
|Chromosome=9
|position=69064991
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FXN
|Gene_s=FXN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=9
|CLNALLE=1
|CLNDBN=Friedreich ataxia 1
|CLNDSDB=OMIM
|CLNDSDBID=229300
|CLNHGVS=NC_000009.11:g.71679907C>G
|CLNORIGIN=0
|CLNSIG=5
|Disease=Friedreich ataxia 1
|FwdALT=G
|FwdREF=C
|GENEINFO=FXN:2395
|GENE_ID=2395
|GENE_NAME=FXN
|REF=C
|RSPOS=71679907
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;NSM;REF;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000a01000002110100
|WGT=1
|dbSNPBuildID=134
|rsid=146818694
}}{{PMID Auto
|PMID=15340363
|Title=Extension of the mutation spectrum in Friedreich's ataxia: detection of an exon deletion and novel missense mutations.
}}