NC_000021.9:g.34223520A>G

  1. Home
  2. NC_000021.9:g.34223520A>G

HGVS Expressions

  • NC_000021.9:g.34223520A>G
Back to search Result
CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

9305545

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608320.G.2.3United Arab EmiratesNA0.145AssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 Study with 914 individuals. 22 SNPs show...
Download Table

Contributors

  • Asha Deepthi: 13.09.2021

Edit History

  • Pratibha Nair: 03.02.2022
  • Asha Deepthi: 11.10.2021
  • Asha Deepthi: 29.09.2021
  • Asha Deepthi: 13.09.2021
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.