NM_000577.4:c.336T>C

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  2. NM_000577.4:c.336T>C

HGVS Expressions

  • NG_021240.1:g.19835T>C
  • NM_000577.4:c.336T>C
  • NP_000568.1:p.Ser112=
  • NC_000002.12:g.113132727T>C

Associated Genes

Interleukin 1 Receptor Antagonist
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

315952

Clinvar

330827

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.2358BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
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Contributors

  • Sami Bizzari: 29.03.2021

Edit History

  • Sami Bizzari: 29.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.