{{Rsnum
|rsid=104894107
|Chromosome=9
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FXN
|position=69064942
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FXN
}}{{omim
|id=606829
|rsnum=104894107
|variant=0005
}}{{ClinVar
|rsid=104894107
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=71679858
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=FXN:2395
|GENE_NAME=FXN
|GENE_ID=2395
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.71679858G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=606829.0005
|CLNSIG=5
|CLNCUI=C0016719
|CLNDBN=Friedreich's ataxia
|Disease=Friedreich's ataxia
|CLNACC=RCV000004189.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0016719:10394003
}}{{PMID Auto
|PMID=9150176
|Title=Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion.
|OA=1
}}

{{PMID Auto
|PMID=9700204
|Title=Maturation of wild-type and mutated frataxin by the mitochondrial processing peptidase.
}}