NM_000583.3:c.58+6190A>G

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HGVS Expressions

  • NG_012837.2:g.32750A>G
  • NM_000583.3:c.58+6190A>G
  • NP_000574.2:p.?
  • NC_000004.12:g.71777771T>C

Associated Genes

Group-Specific Component
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Variant Type

Substitution

dbSNP

1155563

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.40.4United Arab Emirates0.189Osman et al. 2018 328 patients with T2DM
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Contributors

  • Pratibha Nair: 01.06.2022

Edit History

  • Pratibha Nair: 05.12.2022
  • Pratibha Nair: 01.06.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.