NG_011963.2:g.29482A>T

HGVS Expressions

  • NG_011963.2:g.29482A>T
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Genomic Location

chr13:30737959

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.1.5Lebanon1450.45BenignCoronary Heart Disease, Susceptibility to, 1Alwan et al. 2010 From a study of 289 cases with Coronary ...
607339.G.1.6Lebanon1160.45BenignCoronary Heart Disease, Susceptibility to, 1Alwan et al. 2010 From a study of 289 cases with Coronary ...
607339.G.1.7Lebanon1180.44BenignAlwan et al. 2010 From a study of 227 Lebanese controls
607339.G.1.8Lebanon800.44BenignAlwan et al. 2010 From a study of 227 Lebanese controls
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