NM_001384479.1:c.776T>C

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  2. NM_001384479.1:c.776T>C

HGVS Expressions

  • NG_008836.1:g.9543T>C
  • NM_001384479.1:c.776T>C
  • NP_000020.1:p.Met268Thr
  • NC_000001.11:g.230710048A>G

Associated Genes

Angiotensin I
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association, Benign, Protective

Variant Type

Substitution

dbSNP

699

Clinvar

18068

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
106150.G.1.1Lebanon138BenignMajor Depressive DisorderSaab et al. 2007 132 patients testing for association wit...
106150.G.1.2Lebanon134BenignSaab et al. 2007 Healthy control group of 132 first-degre...
145500.G.2.1Lebanon360.44ProtectiveHypertension, EssentialSaab et al. 2011 Study with 124 hypertensive individuals....
145500.G.2.2Lebanon720.44ProtectiveHypertension, EssentialSaab et al. 2011 Study with 124 hypertensive individuals....
145500.G.2.3Lebanon980.54ProtectiveSaab et al. 2011 Study with 146 normotensive individuals
145500.G.2.4Lebanon590.54ProtectiveSaab et al. 2011 Study with 146 normotensive individuals
145500.G.9United Arab Emirates208AssociationHypertension, EssentialFrossard et al. 1998 135 hypertensives (69 females)
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Contributors

  • Pratibha Nair: 05.09.2021
  • Sami Bizzari: 02.03.2021

Edit History

  • Sami Bizzari: 24.01.2024
  • Sayeeda Hana: 13.01.2023
  • Pratibha Nair: 05.09.2021
  • Sami Bizzari: 17.03.2021
  • Sami Bizzari: 03.03.2021
  • Sami Bizzari: 02.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.