NC_000002.12:g.21065449=

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HGVS Expressions

  • NC_000002.12:g.21065449=
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

562338

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 EmiratesNA0.205AssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 Study with 914 individuals. 22 SNPs show...
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Contributors

  • Asha Deepthi: 15.09.2021

Edit History

  • Pratibha Nair: 03.02.2022
  • Asha Deepthi: 11.10.2021
  • Asha Deepthi: 30.09.2021
  • Asha Deepthi: 29.09.2021
  • Asha Deepthi: 15.09.2021
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© CAGS 2024. All rights reserved.