NC_000008.11:g.23923940=

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HGVS Expressions

  • NC_000008.11:g.23923940=
  • NC_000008.11:g.23923940=
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Variant Type

Reference Allele

dbSNP

1705699

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.40.2United Arab Emirates0.242Osman et al. 2018 474 patients with T2DM
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Contributors

  • Pratibha Nair: 31.05.2022

Edit History

  • Pratibha Nair: 31.05.2022
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© CAGS 2024. All rights reserved.