NM_153758.3:c.-35+1984T>G

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HGVS Expressions

  • NG_012088.1:g.4433A>C
  • NM_153758.3:c.-35+1984T>G
  • NC_000001.11:g.206773062T>G

Associated Genes

Interleukin 10
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1800872

Clinvar

16873

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.7184BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
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Contributors

  • Pratibha Nair: 29.03.2021

Edit History

  • Sami Bizzari: 01.06.2021
  • Pratibha Nair: 30.03.2021
  • Pratibha Nair: 29.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.