NM_000537.3:c.98+1161A>G

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HGVS Expressions

  • NG_012122.1:g.6303A>G
  • NM_000537.3:c.98+1161A>G
  • NC_000001.11:g.204165035T>C

Associated Genes

Renin
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

10900556

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
145500.G.8.1United Arab Emirates2280.40AssociationHypertension, EssentialFrossard et al. 1999 280 hypertensives (146 males)
145500.G.8.2United Arab Emirates1680.30Hypertension, EssentialFrossard et al. 1999 274 normotensives (139 males)
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Contributors

  • Pratibha Nair: 05.09.2021

Edit History

  • Asha Deepthi: 12.01.2023
  • Sami Bizzari: 27.12.2022
  • Sayeeda Hana: 06.12.2022
  • Rahila Mir: 03.02.2022
  • Pratibha Nair: 05.09.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.