NM_001645.3:c.*459A>G

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HGVS Expressions

  • NG_012859.1:g.10026A>G
  • NM_001645.3:c.*459A>G
  • NC_000019.10:g.44919689A>G

Associated Genes

Apolipoprotein C-I
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

4420638

Clinvar

162177

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.32.3United Arab EmiratesNA0.160AssociationType 2 Diabetes MellitusOsman et al. 2020 Study with 914 individuals. 36 SNPs show...
608320.G.2.3United Arab EmiratesNA0.160AssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 Study with 914 individuals. 22 SNPs show...
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Contributors

  • Asha Deepthi: 27.09.2021

Edit History

  • Sayeeda Hana: 13.01.2023
  • Asha Deepthi: 30.09.2021
  • Asha Deepthi: 29.09.2021
  • Asha Deepthi: 27.09.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.