{{Rsnum
|rsid=140987490
|Chromosome=9
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FXN
|position=69064936
|Gene_s=FXN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=606829
|variant=0003
|rsnum=140987490
}}{{ClinVar
|rsid=140987490
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=71679852
|CHROM=9
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=FXN:2395
|GENE_NAME=FXN
|GENE_ID=2395
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.71679852A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=606829.0003
|CLNSIG=5
|CLNCUI=C0016719
|CLNDBN=Friedreich's ataxia
|Disease=Friedreich's ataxia
|CLNACC=RCV000004187.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0016719:10394003
}}{{PMID Auto
|PMID=8596916
|Title=Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
}}