{{Rsnum
|rsid=104894108
|Chromosome=9
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FXN
|position=69035785
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FXN
}}{{omim
|id=606829
|rsnum=104894108
|variant=0006
}}{{ClinVar
|rsid=104894108
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=71650701
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=FXN:2395
|GENE_NAME=FXN
|GENE_ID=2395
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000009.11:g.71650701G>T
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000004190.1
|CLNDBN=Friedreich's ataxia
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0016719:10394003
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606829.0006
|Disease=Friedreich's ataxia
}}{{PMID|9090376}} Frataxin fracas.

{{PMID|9737785}} Mutation of the start codon in the FRDA1 gene: linkage analysis of three pedigrees with the ATG to ATT transversion points to a unique common ancestor.

{{PMID|9737785}} Mutation of the start codon in the FRDA1 gene: linkage analysis of three pedigrees with the ATG to ATT transversion points to a unique common ancestor.

{{PMID|10913738}} Mutation detection in an equivocal case of Friedreich's ataxia.