NG_012088.1:g.4206T>C

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HGVS Expressions

  • NG_012088.1:g.4206T>C
  • NC_000001.11:g.206773289T>C

Associated Genes

Interleukin 10
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1800871

Clinvar

1166836

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.7028BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
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Contributors

  • Pratibha Nair: 29.03.2021

Edit History

  • Pratibha Nair: 10.11.2022
  • Pratibha Nair: 30.03.2021
  • Pratibha Nair: 29.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.