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Overall, CAs have preponderance for tandem nucleotide repeat expansions as an etiological factor (10 TREs explain nearly 30\u201340% of ataxia cohort globally). The experience of 10 years of common genetic ataxia subtypes for \u22485600 patients\u2019 referrals (Pan\u2010India) received at a single center is shared herein. Frequencies (in %, n) of SCA types and FRDA in the sample cohort are observed as follows: SCA12 (8.6%, 490); SCA2 (8.5%, 482); SCA1 (4.8%, 272); SCA3 (2%, 113); SCA7 (0.5%, 28); SCA6 (0.1%, 05); SCA17 (0.1%, 05), and FRDA (2.2%, 127). A significant amount of variability in TRE lengths at each locus is observed, we noted presence of biallelic expansion, co\u2010occurrence of SCA\u2010subtypes, and the presence of premutable normal alleles. The frequency of mutated GAA\u2010FRDA allele in healthy controls is 1\/158 (0.63%), thus an expected FRDA prevalence of 1:100 000 persons. The data of this study are relevant not only for clinical decision making but also for guidance in direction of genetic investigations, transancestral comparison of genotypes, and lastly provide insight for policy decision for the consideration of SCAs under rare disease category.<\/jats:p>","DOI":"10.1002\/ggn2.202100078","type":"journal-article","created":{"date-parts":[[2022,3,11]],"date-time":"2022-03-11T01:38:19Z","timestamp":1646962699000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":22,"title":["Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening Tool"],"prefix":"10.1002","volume":"3","author":[{"given":"Pooja","family":"Sharma","sequence":"first","affiliation":[{"name":"Genomics and Molecular Medicine CSIR\u2010Institute of Genomics and Integrative Biology (CSIR\u2010IGIB)  Mall Road Delhi 110007 India"},{"name":"Academy for Scientific and Innovative Research  Ghaziabad 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