NM_001846.2:c.181-27458T>C

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HGVS Expressions

  • NG_032137.1:g.94993T>C
  • NM_001846.2:c.181-27458T>C
  • NP_001837.2:p.?
  • NC_000013.11:g.110397276T>C

Associated Genes

Collagen, Type IV, Alpha-2
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

9515203

Clinvar

1164920

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 EmiratesNA0.165AssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 Study with 914 individuals. 22 SNPs show...
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Contributors

  • Asha Deepthi: 19.09.2021

Edit History

  • Pratibha Nair: 21.11.2022
  • Rahila Mir: 03.02.2022
  • Asha Deepthi: 29.09.2021
  • Asha Deepthi: 19.09.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.