NG_011963.2:g.57503G>A

HGVS Expressions

  • NG_011963.2:g.57503G>A
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Genomic Location

chr13:30765980

CTGA Clinical Significance

Benign

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
607339.G.1.13Lebanon460.1BenignCoronary Heart Disease, Susceptibility to, 1Alwan et al. 2010 From a study of 289 cases with Coronary ...
607339.G.1.14Lebanon100.1BenignCoronary Heart Disease, Susceptibility to, 1Alwan et al. 2010 From a study of 289 cases with Coronary ...
607339.G.1.15Lebanon370.09BenignAlwan et al. 2010 From a study of 227 Lebanese controls
607339.G.1.16Lebanon20.09BenignAlwan et al. 2010 From a study of 227 Lebanese controls
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