NM_018662.3:c.791G>A

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HGVS Expressions

  • NG_011681.2:g.72735G>A
  • NM_018662.3:c.791G>A
  • NP_061132.2:p.Arg264Gln
  • NC_000001.11:g.231694549G>A

Associated Genes

Disrupted in Schizophrenia 1
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

3738401

Clinvar

98346

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
181500.G.1United Arab Emirates430.179BenignMoselhy et al. 2015 121 patients (71 males, 50 females) diag...
181500.G.2United Arab Emirates700.210BenignMoselhy et al. 2015 174 control subjects
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Contributors

  • Pratibha Nair: 29.06.2022

Edit History

  • Pratibha Nair: 29.06.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.