NM_000686.4:c.*199G>T

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  2. NM_000686.4:c.*199G>T

HGVS Expressions

  • NG_016326.1:g.7867G>T
  • NM_000686.4:c.*199G>T
  • NC_000023.11:g.116173571G>T

Associated Genes

Angiotensin II Receptor, Type 2
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

5193

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
603174.G.1LebanonBenignGhassibe-Sabbagh et al. 2012 1110 subjects with CAD
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Contributors

  • Pratibha Nair: 28.03.2021

Edit History

  • Pratibha Nair: 28.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.