{{Rsnum
|rsid=56214919
|Chromosome=9
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FXN
|position=69072646
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FXN
}}{{omim
|id=606829
|rsnum=56214919
|variant=0007
}}

{{ClinVar
|rsid=56214919
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=71687562
|CHROM=9
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050368000000000402110100
|GENEINFO=FXN:2395
|GENE_NAME=FXN
|GENE_ID=2395
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.71687562T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=606829.0007
|CLNSIG=4
|CLNCUI=C0016719
|CLNDBN=Friedreich's ataxia
|Disease=Friedreich's ataxia
|CLNACC=RCV000004191.1
|Tags=PM;PMC;S3D;SLO;HD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0016719:10394003
}}

{{PMID Auto
|PMID=9989622
|Title=Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
}}

{{PMID Auto
|PMID=17703324
|Title=Frataxin gene point mutations in Italian Friedreich ataxia patients.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}