NC_000021.9:g.34223520A>G

HGVS Expressions

  • NC_000021.9:g.34223520A>G
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

9305545

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608320.G.2.3United Arab EmiratesNA0.145AssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 Study with 914 individuals. 22 SNPs show...
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