NM_002187.2:c.*159A>C

HGVS Expressions

  • NG_009618.1:g.19532A>C
  • NM_002187.2:c.*159A>C
  • NP_002178.2:p.?
  • NC_000005.10:g.159315942T>G

Associated Genes

Interleukin 12A
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

3212227

Clinvar

352569

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.25BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
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