NR_135674.1:n.45+8018T>C

HGVS Expressions

  • NC_000017.11:g.48900921A>G

Associated Genes

LOC105371814
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

962272

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608320.G.2.1United Arab EmiratesNA0.453AssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 160 subjects with CAD from a study consi...
608320.G.2.2United Arab EmiratesNA0.328Osman et al. 2020 Group consisting of 332 control subjects...
608320.G.2.3United Arab EmiratesNA0.428AssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 Study with 914 individuals. 22 SNPs show...
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