NG_016779.1:g.4671T>G

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  2. NG_016779.1:g.4671T>G

HGVS Expressions

  • NG_016779.1:g.4671T>G
  • NC_000004.12:g.122456825A>C

Associated Genes

Interleukin 2
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

2069762

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.49BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
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Contributors

  • Pratibha Nair: 29.03.2021

Edit History

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