NM_000789.3:c.2328G>A

HGVS Expressions

  • NG_011648.1:g.16598G>A
  • NM_000789.3:c.2328G>A
  • NP_000780.1:p.Thr776=
  • NC_000017.11:g.63488670G>A
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

4343

Clinvar

256803

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
145500.G.5.1United Arab Emirates610.26AssociationHypertension, EssentialSaeed Mahmood et al. 2003 118 hypertensives (66 males)
145500.G.5.2United Arab Emirates1020.37AssociationSaeed Mahmood et al. 2003 136 normotensives (76 males)
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