NM_000537.3:c.1059+83G>A

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HGVS Expressions

  • NG_012122.1:g.15601G>A
  • NM_000537.3:c.1059+83G>A
  • NP_000528.1:p.?
  • NC_000001.11:g.204155737C>T

Associated Genes

Renin
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

2368564

Clinvar

1239591

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
145500.G.7.1United Arab Emirates3370.51AssociationHypertension, EssentialFrossard et al. 1998 331 hypertensives (167 males)
145500.G.7.2United Arab Emirates2030.36AssociationFrossard et al. 1998 279 hypertensives (141 males)
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Contributors

  • Pratibha Nair: 05.09.2021

Edit History

  • Asha Deepthi: 12.01.2023
  • 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.