NM_001146274.1:c.450+29688T>C

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HGVS Expressions

  • NG_012631.1:g.49063T>C
  • NM_001146274.1:c.450+29688T>C
  • NC_000010.11:g.112994312T>C

Associated Genes

Transcription Factor 7-Like 2
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

34872471

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.14.1Lebanon11980.4AssociationType 2 Diabetes MellitusGhassibe-Sabbagh et al. 2014 Study with 1384 T2DM patients
125853.G.14.2Lebanon13940.4Ghassibe-Sabbagh et al. 2014 Group consisting of 1902 healthy control...
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Contributors

  • Asha Deepthi: 18.02.2021

Edit History

  • Asha Deepthi: 02.06.2021
  • Asha Deepthi: 18.02.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.