NM_001242648.2:c.251-149640A>C

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HGVS Expressions

  • NM_001242648.2:c.251-149640A>C
  • NP_001229577.1:p.?
  • NC_000006.12:g.12903725A>C

Associated Genes

Phosphatase and Actin Regulator 1
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

9349379

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608320.G.1LebanonAssociationCoronary Artery Disease, Autosomal Dominant, 1Hager et al. 2012 Study on 1949 patients with coronary art...
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Contributors

  • Pratibha Nair: 24.06.2020

Edit History

  • Sami Bizzari: 08.06.2021
  • Pratibha Nair: 24.06.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.