NM_000619.2:c.115-483A>T

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HGVS Expressions

  • NG_015840.1:g.6000A>T
  • NM_000619.2:c.115-483A>T
  • NP_000610.2:p.?
  • NC_000012.12:g.68158742T>A

Associated Genes

Interferon, Gamma
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Clinvar Clinical Significance

Protective

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

2430561

Clinvar

14723

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.5BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
145500.G.10.1United Arab Emirates710.46BenignFrossard et al. 2002 70 hypertensives
145500.G.10.2United Arab Emirates620.41BenignFrossard et al. 2002 72 normotensives
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Contributors

  • Pratibha Nair: 05.09.2021
  • Sami Bizzari: 29.03.2021

Edit History

  • Pratibha Nair: 16.01.2023
  • Asha Deepthi: 07.12.2022
  • Pratibha Nair: 05.09.2021
  • Sami Bizzari: 29.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.