NM_000498.3:c.-344T>C

  1. Home
  2. NM_000498.3:c.-344T>C

HGVS Expressions

  • NG_008374.1:g.4660T>C
  • NM_000498.3:c.-344T>C
  • NC_000008.11:g.142918184A>G

Associated Genes

Cytochrome P450, Subfamily XIB, Polypeptide 2
Back to search Result
Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign, Protective

Variant Type

Substitution

dbSNP

1799998

Clinvar

759405

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.37.1United Arab Emirates200.35ProtectiveType 2 Diabetes MellitusAl-Safar et al. 2013b 10 T2DM patients. On its own and in comb...
125853.G.37.2United Arab Emirates520.35BenignType 2 Diabetes MellitusAl-Safar et al. 2013b 52 T2DM patients
125853.G.37.4United Arab Emirates500.44Al-Safar et al. 2013b 25 healthy (control) subjects
125853.G.37.5United Arab Emirates490.44Al-Safar et al. 2013b 49 healthy (control) subjects
Download Table

Contributors

  • Asha Deepthi: 21.04.2022

Edit History

  • Asha Deepthi: 21.04.2022
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.