NG_012088.1:g.3943A>G

HGVS Expressions

  • NG_012088.1:g.3943A>G
  • NC_000001.11:g.206773552T>C

Associated Genes

Interleukin 10
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Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1800896

Clinvar

1710531

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.3679BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
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