NM_004835.4:c.*86A>C

HGVS Expressions

  • NG_008468.1:g.49331A>C
  • NM_004835.4:c.*86A>C
  • NP_004826.5:p.?
  • NC_000003.12:g.148742201A>C

Associated Genes

Angiotensin Receptor 1
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Clinvar Clinical Significance

Benign, Risk factor

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

5186

Clinvar

18065

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
145500.G.2.5Lebanon580.49AssociationHypertension, EssentialSaab et al. 2011 Study with 124 hypertensive individuals....
145500.G.2.6Lebanon640.49AssociationHypertension, EssentialSaab et al. 2011 Study with 124 hypertensive individuals....
145500.G.2.7Lebanon220.25AssociationSaab et al. 2011 Study with 146 normotensive individuals
145500.G.2.8Lebanon520.25AssociationSaab et al. 2011 Study with 146 normotensive individuals
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