NM_015869.4:c.34C>G

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  2. NM_015869.4:c.34C>G

HGVS Expressions

  • NG_011749.1:g.68777C>G
  • NM_015869.4:c.34C>G
  • NP_056953.2:p.Pro12Ala
  • NC_000003.12:g.12351626C>G

Associated Genes

Peroxisome Proliferator-Activated Receptor-Gamma
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Clinvar Clinical Significance

Likely Benign

CTGA Clinical Significance

Association, Likely Benign

Variant Type

Substitution

dbSNP

1801282

Clinvar

130019

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.6.1Lebanon0.102AssociationType 2 Diabetes MellitusMtiraoui et al, 2012 Study with 751 Lebanese T2DM patients
125853.G.6.2Lebanon0.075AssociationMtiraoui et al, 2012 Group consisting of 918 Lebanese control...
125853.G.6.3Tunisia0.084Type 2 Diabetes MellitusMtiraoui et al, 2012 Study with 1470 Tunisian T2DM patients
125853.G.6.4Tunisia0.066Mtiraoui et al, 2012 Group consisting of 838 Tunisian control...
125853.G.30.1United Arab Emirates220.04Likely BenignAl-Safar et al. 2015 272 diabetics. TCF7L2 SNP found to be as...
125853.G.30.2United Arab Emirates190.04Likely BenignAl-Safar et al. 2015 216 control subjects
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Contributors

  • Pratibha Nair: 30.08.2021
  • Asha Deepthi: 20.05.2020

Edit History

  • Pratibha Nair: 30.08.2021
  • Asha Deepthi: 03.06.2021
  • Asha Deepthi: 24.05.2021
  • Asha Deepthi: 21.05.2020
  • Asha Deepthi: 20.05.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.