NM_001146274.1:c.451-10969T>C

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HGVS Expressions

  • NG_012631.1:g.83807T>C
  • NM_001146274.1:c.451-10969T>C
  • NC_000010.11:g.113029056T>C

Associated Genes

Transcription Factor 7-Like 2
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

12243326

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.7.1Lebanon5930.43AssociationType 2 Diabetes MellitusNemr et al, 2012c Study with 691 T2DM patients
125853.G.7.2Lebanon6130.33Nemr et al, 2012c Group consisting of 919 control subjects
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Contributors

  • Asha Deepthi: 20.05.2020

Edit History

  • Asha Deepthi: 25.05.2021
  • Asha Deepthi: 18.02.2021
  • Asha Deepthi: 21.05.2020
  • Asha Deepthi: 20.05.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.