{{Rsnum
|rsid=144610605
|Chromosome=9
|position=69072677
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FXN
|Gene_s=FXN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=G
|CHROM=9
|CLNALLE=1
|CLNDBN=Friedreich ataxia 1
|CLNDSDB=OMIM
|CLNDSDBID=229300
|CLNHGVS=NC_000009.11:g.71687593A>G
|CLNORIGIN=0
|CLNSIG=5
|Disease=Friedreich ataxia 1
|FwdALT=G
|FwdREF=A
|GENEINFO=FXN:2395
|GENE_ID=2395
|GENE_NAME=FXN
|REF=A
|RSPOS=71687593
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;NSM;REF;INT;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368080a01000002110100
|WGT=1
|dbSNPBuildID=134
|rsid=144610605
}}{{PMID Auto
|PMID=9989622
|Title=Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
}}