{{Rsnum
|rsid=104894105
|Chromosome=9
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FXN
|position=69053193
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FXN
}}{{omim
|id=606829
|rsnum=104894105
|variant=0002
}}
{{omim
|id=229300
|rsnum=104894105
}}{{ClinVar
|rsid=104894105
|Reversed=0
|FwdREF=T
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=71668109
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=FXN:2395
|GENE_NAME=FXN
|GENE_ID=2395
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000009.11:g.71668109T>G
|CLNORIGIN=0
|CLNSRCID=
606829.0002
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000004186.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=Friedreich's ataxia
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0016719:10394003
|CLNSRC=OMIM Allelic Variant
|Disease=Friedreich's ataxia
}}{{PMID Auto
|PMID=8596916
|Title=Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
}}

{{PMID Auto
|PMID=9779809
|Title=Identification of a missense mutation in a Friedreich's ataxia patient: implications for diagnosis and carrier studies.
}}