{{Rsnum
|rsid=141526971
|Chromosome=9
|position=69065037
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|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.71679953T>G
|CLNORIGIN=0
|CLNSIG=5
|Disease=Friedreich ataxia 1
|FwdALT=G
|FwdREF=T
|GENEINFO=FXN:2395
|GENE_ID=2395
|GENE_NAME=FXN
|REF=T
|RSPOS=71679953
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;NSM;REF;DSS;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168100a01000002110100
|WGT=1
|dbSNPBuildID=134
|rsid=141526971
}}{{PMID Auto
|PMID=10732799
|Title=The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.
}}