NM_001321868.1:c.*1090T>C

HGVS Expressions

  • NG_023250.3:g.915204T>C
  • NM_001321868.1:c.*1090T>C
  • NP_001308797.1:p.?
  • NC_000007.14:g.18997152T>C

Associated Genes

Histone Deacetylase 9
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

2023938

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 EmiratesNA0.158AssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 Study with 914 individuals. 22 SNPs show...
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