NM_000686.5:c.*501A>C

HGVS Expressions

  • NG_016326.1:g.8169A>C
  • NM_000686.5:c.*501A>C
  • NP_000677.2:p.?
  • NC_000023.11:g.116173873A>C
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CTGA Clinical Significance

Association, Benign

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
300034.G.1.1Lebanon94BenignMajor Depressive DisorderSaab et al. 2007 132 patients testing for association wit...
300034.G.1.2Lebanon95BenignSaab et al. 2007 Healthy control group of 132 first-degre...
608516.G.1.1Lebanon80AssociationMajor Depressive DisorderSaab et al. 2007 132 patients testing for association wit...
608516.G.1.2Lebanon77AssociationSaab et al. 2007 Healthy control group of 132 first-degre...
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