NM_001384479.1:c.593C>T

  1. Home
  2. NM_001384479.1:c.593C>T

HGVS Expressions

  • NG_008836.1:g.9360C>T
  • NM_001384479.1:c.593C>T
  • NP_000020.1:p.Thr207Met
  • NC_000001.11:g.230710231G>A

Associated Genes

Angiotensin I
Back to search Result
Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

4762

Clinvar

296083

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
145500.G.9United Arab Emirates101BenignFrossard et al. 1998 135 hypertensives (69 females)
Download Table

Contributors

  • Pratibha Nair: 05.09.2021

Edit History

  • Sami Bizzari: 24.01.2024
  • Pratibha Nair: 05.09.2021
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.