NM_006457.5:c.*1054del

HGVS Expressions

  • NM_006457.5:c.*1054del
  • NP_006448.5:p.?
  • NC_000004.12:g.94665121del
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CTGA Clinical Significance

Association

Variant Type

Deletion

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
181500.G.1United Arab Emirates860.37AssociationSchizophreniaMoselhy et al. 2015 121 patients (71 males, 50 females) diag...
181500.G.2United Arab Emirates1550.461Moselhy et al. 2015 174 control subjects
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