NM_000418.3:c.1727A>G

HGVS Expressions

  • NG_012086.1:g.54150A>G
  • NM_000418.3:c.1727A>G
  • NP_000409.1:p.Gln576Arg
  • NC_000016.10:g.27363079A>G

Associated Genes

Interleukin 4 Receptor
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Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1801275

Clinvar

14665

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.1762BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
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