NG_011640.1:g.4880C>G

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HGVS Expressions

  • NG_011640.1:g.4880C>G
  • NC_000007.14:g.22727026C>G

Associated Genes

Interleukin 6
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Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1800795

Clinvar

14718

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.6442BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
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Contributors

  • Pratibha Nair: 29.03.2021

Edit History

  • Sami Bizzari: 08.06.2021
  • Pratibha Nair: 30.03.2021
  • Pratibha Nair: 29.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.