{{Rsnum
|rsid=121917850
|Chromosome=8
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TTPA
|position=63064294
|Gene_s=TTPA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121917850
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=63976853
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TTPA:7274
|GENE_NAME=TTPA
|GENE_ID=7274
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.63976853C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000009711.3; RCV000055803.1
|CLNDBN=Ataxia, Friedreich-like, with isolated vitamin E deficiency; Ataxia with vitamin E deficiency
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1241; 600415.0005
|Disease=Ataxia; Ataxia with vitamin E deficiency
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1241:C1848533:277460:96
}}