NM_006457.5:c.*1006A>G

HGVS Expressions

  • NM_006457.5:c.*1006A>G
  • NP_006448.5:p.?
  • NC_000004.12:g.94665073A>G
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

14082

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
181500.G.1United Arab Emirates1180.527AssociationSchizophreniaMoselhy et al. 2015 121 patients (71 males, 50 females) diag...
181500.G.2United Arab Emirates1770.523Moselhy et al. 2015 174 control subjects
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