NG_007462.1:g.4752G>A

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HGVS Expressions

  • NG_007462.1:g.4752G>A

Associated Genes

Tumor Necrosis Factor
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Genomic Location

chr6:31575324

Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Benign, Risk factor

Variant Type

Substitution

dbSNP

361525

Clinvar

1048804

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.0849BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
614389.G.1.11Bahrain1080.15Risk factorPregnancy Loss, Recurrent, Susceptibility to, 1Finan et al. 2010 52 heterozygotes and 4 homozygotes in a ...
614389.G.1.12Bahrain960.1Risk factorFinan et al. 2010 Study of 248 controls
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Contributors

  • Pratibha Nair: 13.05.2020

Edit History

  • Sami Bizzari: 08.06.2021
  • Sami Bizzari: 29.03.2021
  • Pratibha Nair: 13.05.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.