NM_000458.3:c.544+1391T=

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HGVS Expressions

  • NM_000458.3:c.544+1391T=
  • NP_000449.1:p.?
  • NC_000017.11:g.37738049A=

Associated Genes

HNF1 Homeobox B
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

4430796

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.18.1 Lebanon382AssociationType 2 Diabetes MellitusAlmawi et al. 2013 Study with 995 T2DM patients. 382/1186 a...
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Contributors

  • Sami Bizzari: 11.03.2021

Edit History

  • Sami Bizzari: 14.03.2021
  • Sami Bizzari: 11.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.