NM_001178130.2:c.-382A>G

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HGVS Expressions

  • NG_011441.2:g.5071A>G
  • NM_001178130.2:c.-382A>G
  • NP_001171601.1:p.?
  • NC_000004.12:g.109912954A>G
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Clinvar Clinical Significance

Benign, Drug Response

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

4444903

Clinvar

225998

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
145500.G.10.1United Arab Emirates830.58BenignFrossard et al. 2002 70 hypertensives
145500.G.10.2United Arab Emirates750.51BenignFrossard et al. 2002 72 normotensives
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Contributors

  • Pratibha Nair: 05.09.2021

Edit History

  • Asha Deepthi: 07.12.2022
  • Pratibha Nair: 05.09.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.