Emirates NM_000184.3:c.178A>G

HGVS Expressions

  • NG_000007.3:g.43187A>G
  • NM_000184.3:c.178A>G
  • NP_000175.1:p.Lys60Glu
  • NC_000011.10:g.5254429T>C

Associated Genes

Hemoglobin, Gamma G
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CTGA Clinical Significance

Benign

Variant Type

Substitution

Clinvar

14997

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
141749.1United Arab Emirates1BenignAbbes et al. 1995
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