NR_003529.3:n.2449-316A>G

  1. Home
  2. NR_003529.3:n.2449-316A>G

HGVS Expressions

  • NR_003529.3:n.2449-316A>G
  • NC_000009.12:g.22096056A>G

Associated Genes

CDKN2B Antisense RNA
Back to search Result
Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Likely Benign

Variant Type

Substitution

dbSNP

10757274

Clinvar

812640

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.34.1United Arab Emirates3980.58Likely BenignType 2 Diabetes MellitusBaalfaqih et al. 2020 341 T2DM patients without coronary arter...
125853.G.34.2United Arab Emirates1980.56Likely BenignType 2 Diabetes MellitusBaalfaqih et al. 2020 178 T2DM patients with coronary artery d...
125853.G.34.3United Arab Emirates4930.55Baalfaqih et al. 2020 Group consisting of 450 control subjects...
Download Table

Contributors

  • Asha Deepthi: 18.03.2022

Edit History

  • Pratibha Nair: 16.01.2023
  • Asha Deepthi: 21.03.2022
  • Asha Deepthi: 18.03.2022
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.